Process for the preparation of pesticides

The invention relates to a process for the preparation of compounds of the formula ##STR2## and, where appropriate, their tautomers, in each case in the free form or salt form, in which either
X is CH or N, Y is OR.sub.1 and Z is O, or
X is N, Y is NHR.sub.8 and Z is O, S or S(.dbd.O);
R.sub.1 is C.sub.1 -C.sub.4 alkyl;
R.sub.2 is H, C.sub.1 -C.sub.4 alkyl, halogeno-C.sub.1 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl or C.sub.1 -C.sub.4 alkoxymethyl;
R.sub.3 and R.sub.4 independently of one another are H, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, OH, CN, NO.sub.2, a (C.sub.1 -C.sub.4 alkyl).sub.3 --Si group, where the alkyl groups can be identical or different, halogen, (C.sub.1 -C.sub.4 alkyl)S(.dbd.O).sub.m, (halogeno-C.sub.1 -C.sub.4 alkyl)S(.dbd.O).sub.m, halogeno-C.sub.1 -C.sub.4 alkyl or halogeno-C.sub.1 -C.sub.4 alkoxy;
R.sub.5 is C.sub.1 -C.sub.6 alkyl, halogeno-C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, halogeno-C.sub.1 -C.sub.6 alkoxy, C.sub.1 -C.sub.6 -alkylthio, halogen-C.sub.1 -C.sub.6 alkylthio, C.sub.1 -C.sub.6 alkylsulfinyl, halogeno-C.sub.1 -C.sub.6 -alkylsulfinyl, C.sub.1 -C.sub.6 alkylsulfonyl, halogeno-C.sub.1 -C.sub.6 alkylsulfonyl, C.sub.1 -C.sub.6 alkoxy-C.sub.1 -C.sub.6 alkyl, halogeno-C.sub.1 -C.sub.6 alkoxy C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkylthio-C.sub.1 -C.sub.6 alkyl, halogeno-C.sub.1 -C.sub.6 alkylthio-C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkylsulfinyl-C.sub.1 -C.sub.6 alkyl, halogeno-C.sub.1 -C.sub.6 -alkylsulfinyl-C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 -alkylsulfonyl-C.sub.1 -C.sub.6 alkyl, halogeno-C.sub.1 -C.sub.6 -alkylsulfonyl-C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 -alkylcarbonyl, halogeno-C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkoxycarbonyl, halogeno-C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.4 -alkoxyiminomethyl; di(C.sub.1 -C.sub.6 alkyl)-aminocarbonyl, where the alkyl groups can be identical or different; C.sub.1 -C.sub.6 -alkylaminothiocarbonyl; di(C.sub.1 -C.sub.6 alkyl)-aminothiocarbonyl, where the alkyl groups can be identical or different; C.sub.1 -C.sub.6 -alkylamino, di(C.sub.1 -C.sub.6 alkyl)-amino, where the alkyl groups can be identical or different; halogen, NO.sub.2, CN, SF.sub.5, thioamido, thiocyanatomethyl; an unsubstituted or mono- to tetrasubstituted C.sub.1 -C.sub.4 alkylenedioxy group, where the substituents are selected from the group consisting of C.sub.1 -C.sub.4 alkyl and halogen; or QR.sub.6, where, if n is greater than 1, the radicals R.sub.5 can be identical or different;
R.sub.6 is C.sub.2 -C.sub.6 alkenyl or C.sub.2 -C.sub.6 alkynyl which are unsubstituted or substituted by 1 to 3 halogen atoms; (C.sub.1 -C.sub.4 alkyl).sub.3 Si, where the alkyl groups can be identical or different; CN; or an unsubstituted or mono- to pentasubstituted C.sub.3 -C.sub.6 cycloalkyl, aryl or heterocyclyl group, where the substituents are selected from the group consisting of halogen, C.sub.1 -C.sub.6 alkyl, halogeno-C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, halogeno-C.sub.1 -C.sub.6 alkoxy, phenoxy, naphthoxy and CN;
A either is a direct bond, C.sub.1 -C.sub.10 alkylene, --C(.dbd.O)--,--C(.dbd.S)-- or halogeno-C.sub.1 -C.sub.10 alkylene and R.sub.7 is a radical R.sub.10, or is C.sub.1 -C.sub.10 alkylene, --C(.dbd.O)--,--C(.dbd.S)-- or halogeno-C.sub.1 -C.sub.10 alkylene and R.sub.7 is OR.sub.10, N(R.sub.10).sub.2, where the radicals R.sub.10 can be identical or different, or --S(.dbd.O).sub.q R.sub.10 ;
R.sub.8 is H or C.sub.1 -C.sub.4 alkyl;
R.sub.9 is methyl, fluoromethyl or difluoromethyl;
R.sub.10 is H; an unsubstituted or substituted C.sub.1 -C.sub.6 alkyl, C.sub.2 -C.sub.6 alkenyl or C.sub.2 -C.sub.6 alkynyl group, where the substituents are selected from the group consisting of halogen; (C.sub.1 -C.sub.4 alkyl).sub.3 Si, where the alkyl groups can be identical or different; C.sub.3 -C.sub.6 cyclo-alkyl, which is unsubstituted or substituted by halogen; C.sub.1 -C.sub.6 alkoxycarbonyl, which is unsubstituted or substituted by halogen; unsubstituted or substituted aryl, where the substituents are selected from the group consisting of halogen, halogeno-C.sub.1 -C.sub.4 alkyl and CN; a (C.sub.1 -C.sub.4 alkyl).sub.3 Si group, where the alkyl groups can be identical or different; C.sub.3 -C.sub.6 cycloalkyl, which is unsubstituted or substituted by halogen; C.sub.1 -C.sub.6 alkoxycarbonyl which is unsubstituted or substituted by halogen; or an unsubstituted or substituted aryl or heterocyclyl group, where the substituents are selected from the group consisting of halogen and halogeno-C.sub.1 -C.sub.4 alkyl;
Q is a direct bond, C.sub.1 -C.sub.8 alkylene, C.sub.2 -C.sub.6 alkenylene, C.sub.2 -C.sub.6 alkynylene, O, O(C.sub.1 -C.sub.6 alkylene), (C.sub.1 -C.sub.6 alkylene)O, S(.dbd.O).sub.p, S(.dbd.O).sub.p (C.sub.1 -C.sub.6 alkylene) or (C.sub.1 -C.sub.6 alkylene)S(.dbd.O).sub.p ;
m is 0, 1 or 2;
n is 0, 1, 2, 3, 4 or 5;
p is 0, 1 or 2; and
q is 0, 1 or 2,
and the C.dbd.N double bond marked with E has the E configuration,
which comprises
a1) reacting either a compound of the formula ##STR3## in which A, R.sub.2, R.sub.5, R.sub.7 and n are as defined for formula I and the C.dbd.N double bond marked with E has the E configuration, or a tautomer thereof, in each case in the free form or in salt form, if appropriate in the presence of a base, with a compound of the formula ##STR4## which is known or can be prepared by methods known per se and in which X, Y, Z, R.sub.3, R.sub.4 and R.sub.9 are as defined for formula I and X.sub.1 is a leaving group, or a tautomer thereof, in each case in the free from or in salt form, or
a2) reacting a compound of the formula ##STR5## in which A, R.sub.2, R.sub.5, R.sub.7 and n are as defined for formula I and the C.dbd.N double bond marked with E has the E configuration, or a tautomer thereof, in each case in the free form or in the salt form, if appropriate in the presence of a base, with a compound of the formula ##STR6## which is known or can be prepared by methods known per se and in which X, Y, Z, R.sub.3, R.sub.4 and R.sub.9 are as defined for formula I, or a tautomer thereof, in each case in the free form or in salt form, or
b1) reacting a compound of the formula ##STR7## in which R.sub.2, R.sub.5 and n are as defined for formula I and the C.dbd.N double bond marked with E has the E configuration, or a tautomer thereof, in each case in the free form or in salt form, if appropriate in the presence of a base, with a compound of the formula
R.sub.7 --A--X.sub.2 (VII),
which is known or can be prepared by methods known per se and in which A and R.sub.7 are as defined for formula I and X.sub.2 is a leaving group, and either further reacting the compound thus obtainable, of the formula IV, for example according to method a2), or
b2) reacting it with hydroxylamine or a salt thereof, if appropriate in the presence of a base or acid catalyst, and further reacting the compound thus obtainable, of the formula II, for example according to method a1), or
c) reacting a compound of the formula ##STR8## which is known or can be prepared by methods known per se and in which R.sub.2, R.sub.5 and n are as defined for formula I, or a tautomer thereof, in each case in the free form or in salt form, if appropriate in the presence of a base, with a C.sub.1 -C.sub.6 alkyl nitrite, and further reacting the compound thus obtainable, of the formula VI, for example according to method b),
the E isomers of the compounds of the formulae II, IV and VI, or a tautomer thereof, in each case in the free form or in salt form, a process for their preparation and their use for the preparation of compounds of the formula I.
The compounds of the formula I are known pesticides. The processes known to date for their preparation give mixtures of E and Z isomers in respect of the C.dbd.N double bond marked with E in formula I of different composition, depending on the process. Since the biological properties of the E isomers are in each case found to be superior to those of the mixtures and of the Z isomers, there is a need to develop preparation processes for compounds of the formula I having the isomerically pure E configuration. This object is achieved by the preparation process according to the invention.
Unless defined differently, the general terms used above and below are defined as follows.
Carbon-containing groups and compounds in each case contain 1 up to and including 8, preferably 1 up to and including 6, in particular 1 up to and including 4, especially 1 or 2, carbon atoms.
Alkyl--as a group per se and as a structural element of other groups and compounds, such as of halogenoalkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylcarbonyl, alkoxycarbonyl, halogenoalkoxycarbonyl, alkylaminocarbonyl, alkoxyiminomethyl, alkylaminothiocarbonyl and alkylamino--is, in each case taking into due consideration the number, included from case to case, of carbon atoms contained in the corresponding group or compound, either straight-chain, i.e. methyl, ethyl, propyl, butyl, pentyl or hexyl, or branched, for example isopropyl, isobutyl, sec-butyl, tert-butyl, isopentyl, neopentyl or isohexyl.
Alkenyl--as a group per se and as a structural element of other groups and compounds, such as of halogenoalkenyl--is, in each case under due consideration of the number, included from case to case, of carbon atoms contained in the corresponding group or compound, either straight-chain, for example vinyl, 1-methylvinyl, allyl, 1-butenyl or 2-hexenyl, or branched, for example iso-propenyl.
Alkynyl--as a group per se and as a structural element of other groups and compounds, such as of halogenoalkynyl--is, in each case under due consideration of the number, included from case to case, of carbon atoms contained in the corresponding group or compound, either straight-chain, for example propargyl, 2-butynyl or 5-hexynyl, or branched, for example 2-ethynylpropyl or 2-propargylisopropyl.
C.sub.3 -C.sub.6 cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
Alkylene--as a group per se and as a structural element of other groups and compounds, such as of O(alkylene), (alkylene)O, S(.dbd.O).sub.p (alkylene), (alkylene)S(.dbd.O).sub.p or alkylenedioxy--is, in each case under due consideration of the number, included from case to case, of carbon atoms contained in the corresponding group or compound, either straight-chain, for example --CH.sub.2 CH.sub.2 --, --CH.sub.2 CH.sub.2 CH.sub.2 -- or --CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 --, or branched, for example --CH(CH.sub.3)--, --CH(C.sub.2 H.sub.5)--, --C(CH.sub.3).sub.2 --, --CH(CH.sub.3)CH.sub.2 -- or --CH(CH.sub.3)CH(CH.sub.3)--.
Alkenylene is, in each case under due consideration of the number, from case to case, of carbon atoms contained in the corresponding compound, either straight-chain, for example vin-1,2-ylene, all-1,3-ylene, but-1-en-1,4-ylene or hex-2-en-1,6-ylene, or branched, for example 1-methylvin-1,2-ylene.
Alkynylene is, in each case under due consideration of the number, from case to case, of carbon atoms contained in the corresponding compound, either straight-chain, for example propargylene, 2-butynylene or 5-hexynylene, or branched, for example 2-ethynylpropylene or 2-propargylisopropylene.
Aryl is phenyl or naphthyl, in particular phenyl.
Heterocyclyl is a 5- to 7-membered aromatic or non-aromatic ring having one to three heteroatoms, which are selected from the group consisting of N, O and S. 5- and 6-membered rings which contain a nitrogen atom as a heteroatom and, if appropriate, a further heteroatom, preferably nitrogen or sulfur, in particular nitrogen, are preferred.
Halogen--as a group per se and as a structural element of other groups and compounds, such as of halogenoalkyl, halogenoalkenyl and halogenoalkynyl--is fluorine, chlorine, bromine or iodine, especially fluorine, chlorine or bromine, in particular fluorine or chlorine, very especially fluorine.
Halogen-substituted carbon-containing groups and compounds, such as halogenoalkyl, halogenoalkenyl or halogenoalkynyl, can be partly halogenated or perhalogenated, and in the case of polyhalogenation, the halogen substituents can be identical or different. Examples of halogenoalkyl--as a group per se and as a structural element of other groups and compounds, such as of halogenoalkenyl--are methyl which is mono- to trisubstituted by fluorine, chlorine and/or bromine, such as CHF.sub.2 or CF.sub.3 ; ethyl which is mono- to pentasubstituted by fluorine, chlorine and/or bromine, such as CH.sub.2 CF.sub.3, CF.sub.2 CF.sub.3, CF.sub.2 CCl.sub.3, CF.sub.2 CHCl.sub.2, CF.sub.2 CHF.sub.2, CF.sub.2 CFCl.sub.2, CF.sub.2 CHBr.sub.2, CF.sub.2 CHClF, CF.sub.2 CHBrF or CClFCHClF; propyl or isopropyl which is mono- to heptasubstituted by fluorine, chlorine and/or bromine, such as CH.sub.2 CHBrCH.sub.2 Br, CF.sub.2 CHFCF.sub.3, CH.sub.2 CF.sub.2 CF.sub.3 or CH(CF.sub.3).sub.2 ; and butyl or one of its isomers which is mono- to nonasubstituted by fluorine, chlorine and/or bromine, such as CF(CF.sub.3)--CHFCF.sub.3 or CH.sub.2 (CF.sub.2).sub.2 CF.sub.3. Halogenoalkenyl is, for example, CH.sub.2 CH.dbd.CHCl, CH.sub.2 CH.dbd.CCl.sub.2, CH.sub.2 CF.dbd.CF.sub.2 or CH.sub.2 CH.dbd.CHCH.sub.2 Br. Halogenoalkynyl is, for example, CH.sub.2 C.tbd.CF, CH.sub.2 C.tbd.CCH.sub.2 Cl or CF.sub.2 CF.sub.2 C.tbd.CCH.sub.2 F.
Some compounds I to VI and VIII can be present as tautomers, as is familiar to the expert, in particular if AR.sub.7 is H. Compounds I above and below are therefore also to be understood as meaning corresponding tautomers, even if the latter are not mentioned specifically in each case.
Compounds I to VI and VIII which contain at least one basic centre, can form, for example, acid addition salts. These are formed, for example, with strong inorganic acids, such as mineral acids, for example perchloric acid, sulfuric acid, nitric acid, nitrous acid, a phosphoric acid, or a hydrogen halide acid, with strong inorganic carboxylic acids, such as C.sub.1 -C.sub.4 alkanecarboxylic acids which are unsubstituted or substituted, for example by halogen, for example acetic acid, such as dicarboxylic acids which are saturated or unsaturated, for example oxalic, malonic, succinic, maleic, fumaric or phthalic acid, such as hydroxycarboxylic acids, for example ascorbic, lactic, malic, tartaric or citric acid, or such as benzoic acid, or with organic sulfonic acids, such as C.sub.1 -C.sub.4 alkane- or arylsulfonic acids which are unsubstituted or substituted, for example by halogen, for example methane- or p-toluenesulfonic acid. Compounds I with at least one acid group can furthermore form salts with bases. Suitable salts with bases are, for example, metal salts such as alkali metal or alkaline earth metal salts, for example sodium, potassium or magnesium salts, or salts with ammonia or an organic amine, such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower alkylamine, for example ethyl-, diethyl-, triethyl- or dimethyl-propyl-amine, or a mono-, di- or trihydroxy-lower alkylamine, for example mono-, di- or triethanolamine. Furthermore, where appropriate, corresponding inner salts can be formed. Agrochemically advantageous salts are preferred in the context of the invention; however, salts which have disadvantages for agrochemical uses, for example salts which are toxic to bees or fish, which are employed, for example, for isolation or purification of free compounds I or agrochemically usable salts thereof, are also included. Compounds of the formulae I to VI and VIII in the free form and in the form of their salts are also to be understood above and below as meaning the corresponding salts or the free compounds I to VI and VIII. The same applies to tautomers of compounds of the formulae I to VI and VIII and salts thereof. In general, the free form is in each case preferred.
The reactions described above and below are carried out in a manner known per se, for example in the absence or usually in the presence of a suitable solvent or diluent or a mixture thereof, the reaction being carried out, as required, with cooling, at room temperature or with heating, for example in a temperature range from about -80.degree. C. up to the boiling point of the reaction medium, preferably from about 0.degree. C. up to about 150.degree. C., and, if necessary, in a closed vessel, under pressure, in an inert gas atmosphere and/or under anhydrous conditions. Particularly advantageous reaction conditions can be seen from the examples.
The starting materials mentioned above and below, which are used for the preparation of the compounds I, in each case in the free form or in salt form, are known or can be prepared by methods known per se, for example in accordance with the following statements.
Variants a1/a2)
Suitable leaving groups X.sub.1 in compounds III are, for example, hydroxyl, C.sub.1 -C.sub.8 alkoxy, halogeno-C.sub.1 -C.sub.8 alkoxy, C.sub.1 -C.sub.8 alkanoyloxy, mercapto, C.sub.1 -C.sub.8 alkylthio, halogeno-C.sub.1 -C.sub.8 alkylthio, C.sub.1 -C.sub.8 alkanesulfonyloxy, halogeno-C.sub.1 -C.sub.8 alkanesulfonyloxy, benzenesulfonyloxy, toluenesulfonyloxy and halogen, preferably toluenesulfonyloxy, trifluoromethanesulfonyloxy and halogen, in particular halogen.
Suitable bases for facilitating the reaction are, for example, alkali metal or alkaline earth metal hydroxides, hydrides, amides, alkanolates, acetates, carbonates, dialkylamides or alkylsilylamides, alkylamines, alkylenediamines, N-alkylated or non-alkylated, saturated or unsaturated cycloalkylamines, basic heterocyclic compounds, ammonium hydroxides and carbocyclic amines. Examples are sodium hydroxide, hydride, amide, methanolate, acetate and carbonate, potassium tert-butanolate, hydroxide, carbonate, and hydride, lithium diisopropylamide, potassium bis(trimethylsilyl)amide, calcium hydride, triethylamine, diisopropyl-ethyl-amine, triethylenediamine, cyclohexylamine, N-cyclohexyl-N,N-dimethyl-amine, N,N-diethylaniline, pyridine, 4-(N,N-dimethylamino)pyridine, quinuclidine, N-methylmorpholine, benzyl-trimethyl-ammonium hydroxide and 1,5-diazabicyclo[5.4.0]undec-5-ene (DBU).
The reaction partners can be reacted with one another as such, i.e. without addition of a solvent or diluent, for example in the melt. However, the addition of an inert solvent or diluent or of a mixture thereof is usually advantageous. Examples of such solvents or diluents are: aromatic, aliphatic and alicyclic hydrocarbons and halogenohydrocarbons, such as benzene, toluene, xylene, mesitylene, tetralin, chlorobenzene, dichlorobenzene, bromobenzene, petroleum ether, hexane, cyclohexane, methylene chloride, chloroform, carbon tetrachloride, dichloroethane, trichloroethene or tetrachloroethene; esters, such as ethyl acetate; ethers, such as diethyl ether, dipropyl ether, diisopropyl ether, dibutyl ether, tert-butyl methyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol dimethyl ether, dimethoxydiethyl ether, tetrahydrofuran or dioxane; ketones, such as acetone, methyl ethyl ketone or methyl isobutyl ketone; alcohols, such as methanol, ethanol, propanol, isopropanol, butanol, ethylene glycol or glycerol; amides, such as N,N-dimethylformamide, N,N-diethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone or hexamethylphosphoric acid triamide; nitriles such as acetonitrile or propionitrile; and sulfoxides, such as dimethyl sulfoxide. If the reaction is carried out in the presence of a base, bases employed in excess, such as triethylamine, pyridine, N-methylmorpholine or N,N-diethylaniline, can also serve as the solvent or diluent.
The reaction is advantageously carried out in a temperature range from about 0.degree. C. up to about 180.degree. C., preferably from about 10.degree. C. up to about 80.degree. C., in many cases in the range between room temperature and the reflux temperature of the reaction mixture.
The reaction is preferably carried out under normal pressure.
The reaction can be carried out without an inert gas atmosphere; preferably, however, it is carried out under an inert gas atmosphere, for example nitrogen or argon, in particular nitrogen.
The reaction time is not critical; a reaction time of about 0.1 to about 24 hours, in particular about 0.5 to about 2 hours, is preferred.
The product is isolated by customary methods, for example by filtration, crystallization, distillation or chromatography or any suitable combination of these processes.
In a preferred embodiment of variants a1/a2), a compound II is reacted with a compound III at 0.degree. C. to 80.degree. C., preferably 10.degree. C. to 30.degree. C., in an inert solvent, preferably an amide, in particular N,N-dimethylformamide in the presence of a metal hydride, preferably sodium hydride.
Particularly preferred conditions for the reaction are described in Examples H 1d) and H 3f).
The compounds of the formula III are known or can be prepared analogously to known compounds.
The compounds I are known. However, their preparation according to the prior art has a large number of serious industrial, ecological, economic and other disadvantages.
Thus, in the preparation processes according to the prior art, as a rule E/Z isomer mixtures with respect to the C.dbd.N double bond marked with E in formula I are obtained. Since the biological properties of the E isomers are in each case found to be superior to those of the mixtures and of the Z isomers in each case, the processes according to the prior art have the significant disadvantage that products are produced which are either significantly less active as E/Z mixtures or from which the Z isomers must be removed in order to increase their biological activity, which means that many unnecessary handling operations must be carried out for separation of isomers, which has the effect of being very time-consuming, blocks valuable production lines for a long time and is associated with high additional energy costs. The removal of the less active Z isomer also leads to additional enormous losses in yield, which in turn not only is problematic and ecologically disadvantageous, but also renders the process according to the prior art much more expensive and consequently economically of no interest. The industrial, ecological, economic and other disadvantages of the processes according to the prior art are not limited to those described above, these latter being intended to serve only as a few examples of the large number of disadvantages of the processes according to the prior art. The disadvantages of the processes according to the prior art cause serious problems even when the processes are carried out on a laboratory scale. When the processes are carried out on a larger scale, these disadvantages intensify considerably. In the end, however, the aim is to carry out a specific process on an industrial scale if this process is to be suitable for preparing products for agrochemical purposes.
According to the process of the present invention, the compounds I are prepared by reaction of the compound II with a compound III or by reaction of the compound IV with a compound V. These processes according to the invention have extremely surprising industrial, ecological, economic and other advantages compared with the processes from the prior art. Since the compounds II or, respectively, IV are present in the preparation process according to the invention as pure E isomers in respect of the C.dbd.N double bond marked with E, only the E isomer of the compounds I is produced in the present process, which has the effect of an enormous saving in time and at the same time a high saving in cost and energy, since no valuable production lines are blocked for a long time for separation of the isomers, and at the same time the amount of biologically more active E isomer produced by per unit time is much higher than in the processes according to the prior art. The resources such as starting products and energy are consequently utilized to the optimum in the present process, which not only very greatly simplifies the process and renders it ecologically advantageous, but consequently renders it cheaper and therefore of greater economic interest. This means that all the disadvantages of the processes according to the prior art which can be attributed to the formation of E/Z isomers are avoided. The industrial, ecological, economic and other advantages of the process according to the invention are not limited only to those described above, these latter being intended to serve only as a few examples of the large number of advantages inherent in this process. Due to all the abovementioned advantages of the present process, the serious problems which occur in the processes according to the prior art are avoided even at the stage of a laboratory process. If the present process is used on a larger scale, these advantages prove to be even much more significant, which has the effect that these advantages first allow the process to be used on an industrial scale.
For this reason, all the industrial, ecological, economic and other disadvantages of the processes according to the prior art are surprisingly advantageously overcome in the preparation of compounds I by the present process.
Variant b)
The process according to variant b) is carried out by first reacting compound VI with compound VII, if appropriate further reacting the resulting product IV, if appropriate after isolation, with hydroxylamine or a salt thereof, and further reacting the resulting products II or, respectively, IV, if appropriate after isolation, in accordance with variants a1/a2), for example in the manner described above, to give the compounds I.
Suitable leaving groups X.sub.2 in the compounds VII are, for example, those which are mentioned as examples for X.sub.1 in variants a1/a2).
Suitable bases for facilitating the reaction are, for example, those which are mentioned in variants a1/a2).
The reaction partners can be reacted with one another as such, i.e. without addition of a solvent or diluent, for example in the melt. However, the addition of an inert solvent or diluent or of a mixture thereof is usually advantageous. Examples of such solvents or diluents are those mentioned in variants a1/a2).
The reaction is advantageously carried out in a temperature range from about 0.degree. C. to about 180.degree. C., preferably from about 10.degree. C. to about 80.degree. C., in many cases in the range between room temperature and the reflux temperature of the reaction mixture.
The reaction is preferably carried out under normal pressure.
The reaction can be carried out without an inert gas atmosphere; preferably, however, it is carried out under an inert gas atmosphere, for example nitrogen or argon, in particular nitrogen.
The reaction time is not critical; a reaction time of about 0.1 to about 24 hours, in particular about 0.5 to about 5 hours, is preferred.
The product is isolated by customary methods, for example filtration, crystallization, distillation or chromatography or any suitable combination of these processes.
In a preferred embodiment of variant b), a compound VI is reacted with a compound VII at 0.degree. C. to 80.degree. C., preferably 10.degree. C. to 60.degree. C., in an inert solvent, preferably a nitrile, in particular acetonitrile, in the presence of a metal carbonate, preferably potassium carbonate, and the compound IV thus obtainable is then further reacted, preferably in accordance with method a2).
Particularly preferred conditions for the reaction are described in Examples H 1b) to 1d) and H 3d) to 3f).
The compounds of the formula VII are known or can be prepared analogously to known compounds.
The present process according to the invention of variant b), which in principle is an advantageous combination of an O-alkylation reaction with process variants a1/a2) according to the invention, has all the great advantages compared with the prior art which have already been discussed above for the process according to the invention of variants a1/a2). In particular, the process of variant b) ensures that the E configuration of the C.dbd.N double bond marked with E in compound VI is retained. Furthermore, however, the process according to the invention of variant b) also has further industrial, ecological, economic and other advantages which are connected with the specific property that the intermediate product IV initially formed is not purified but is directly further processed as the moist crude product, in the case of intermediate isolation, or in situ in the reaction mixture, if it is not isolated. This missing purification step on the intermediate product mentioned is of advantage, for example, in as much as it is not necessary to dry it, which not only saves energy and further resources, but also enormously increases the safety of the preparation process, since the possible danger of a dust explosion of the dry intermediate product is averted completely. The savings in resources are even greater if the intermediate product is further reacted without purification, since, for example, no additional solvents are consumed for the recrystallization. The process of variant b) is of particular advantage compared with the individual process steps of the alkylation reaction of variants a1/a2) carried out in that the total reaction time in the process of variant b) is much shorter, which consequently leads to a much higher production of reaction product I per unit time and therefore to a much more efficient utilization of the valuable production lines. Furthermore, the total yield of reaction product I is surprisingly good when the process of variant b) is employed, and, compared with the combined yields of the individual process steps of the alkylation reaction and variants a1/a2) carried out, is in the same percentage range or even beffer. The industrial, ecological, economic and other advantages of the process according to the invention of variant b) are not limited to those described above, these latter being intended to serve only as a few examples of the large number of advantages inherent in the process according to the invention of variant b).
By using process variant b) according to the invention for preparation of the compounds I, a large number of industrial, ecological, economic and other advantages can therefore surprisingly be utilized efficiently.
Variant c)
The process according to variant c) is carried out by first reacting compound VIII with an alkylnitrite and further reacting the resulting product VI, if appropriate after isolation, in accordance with variant b), for example in the manner described above, to give the compounds I.
Suitable bases for facilitating the reaction are, for example, those which are mentioned in variants a1/a2).
The reaction partners can be reacted with one another as such, i.e. without addition of a solvent or diluent, for example in the melt. However, the addition of an inert solvent or diluent or of a mixture thereof is usually advantageous. Examples of such solvents or diluents are those mentioned in variants a1/a2).
The reaction is advantageously carried out in a temperature range from about 0.degree. C. to about 180.degree. C., preferably from about 0.degree. C. to about 60.degree. C., in many cases in the range between room temperature and the reflux temperature of the reaction mixture.
The reaction is preferably carried out under normal pressure.
The reaction can be carried out without an inert gas atmosphere; preferably, however, it is carried out under an inert gas atmosphere, for example nitrogen or argon, in particular nitrogen.
The reaction time is not critical; a reaction time of about 0.1 to about 24 hours, in particular about 0.5 to about 3 hours, is preferred.
The product is isolated by customary methods, for example filtration, crystallization, distillation or chromatography or any suitable combination of these processes.
In a preferred embodiment of variant c), a compound VIII is reacted with an alkyl nitrite at 0.degree. C. to 80.degree. C., preferably 0.degree. C. to 40.degree. C., in an inert solvent, preferably an alcohol, in particular methanol, in the presence of a metal alcoholate, preferably sodium methanolate, and the compound VI thus obtainable is then further reacted, preferably in accordance with method b).
Particularly preferred conditions for the reactions are described in Examples H 3d) to 3f).
The compounds of the formula VIII are known or can be prepared analogously to known compounds.
The present process according to the invention of variant c), which in principle is an advantageous combination of an oximation reaction with process variants a1/a2) and b) according to the invention, has all the great advantages compared with the prior art which have already been discussed above for the processes according to the invention of variants a1/a2) and b). Furthermore, the present oximation process for the preparation of the compounds VI surprisingly result exclusively in the E configuration of the C.dbd.N double bond marked with E in formula VI. It is thus ensured that the particular starting products II, IV or, respectively, VI in the subsequent processes according to the invention for the preparation of the compounds I, for example in process variants a1/a2) and b), are pure E isomers.
A large number of industrial, ecological, economic and other advantages can therefore surprisingly be utilized efficiently by using process variants c) according to the Invention for the preparation of the compounds of the formula I.
The E isomers of the compounds of the formulae II, IV and VI and tautomers thereof, in each case in the free form or in salt form, are novel and the present invention likewise relates to them.
The present invention furthermore relates to a process for the preparation of the E isomers of a compound of the formula VI or of a tautomer thereof, in each case in the free form or in salt form, according to the abovementioned process c),
a process for the preparation of the E isomers of a compound of the formula IV, or of a tautomer thereof, in each case in the free form or in salt form, according to the abovementioned process b1), and
a process for the preparation of the E isomers of a compound of the formula II, or of a tautomer thereof, in each case in the free form or in salt form, according to the abovementioned process b2).
The process conditions for the preparation of these intermediate products can be seen from the abovementioned processes a), b) and c).

PREPARATION EXAMPLE
Example H1
Methyl 2-[[[(1-methyl-2-phenyl-2-E-[(2-propynyl)oxyimino]-ethylidene)amino]oxy]methyl].alpha.-(methoxymethylene)-phenylacetate (Compound 1.16)
H1a) 1-Phenyl-1,2-propanedione 1-E-oxime
69.7 g of a 30% solution of sodium methylate in methanol are added dropwise to a solution of 40.2 g of 1-phenyl-2-propanone and 36.1 g of isopentyl nitrite in 460 ml of methanol at 20-25.degree., while cooling. The reaction mixture is then further stirred at room temperature for 1 hour. After the solution has been concentrated in vacuo, the residue is dissolved in 600 ml of water, the solution is acidified with 10% hydrochloric acid, the product which precipitates out is filtered off and dissolved in ethyl acetate and the organic phase is washed twice with water, dried with sodium sulfate and evaporated in vacuo. The residue is stirred up in hexane and filtered. The title product is thus obtained with a melting of 168-70.degree. C.
H1b) 1-Phenyl-1,2-propanedione 1-E-[(2-propynyl)oxime]
A mixture of 14 g of 1-phenyl-1,2-propanedione 1-E-oxime, 11.9 g of 1-bromo-2-propyne, 13.8 g of potassium carbonate and 0.5 g of potassium iodide in 170 ml of acetonitrile is stirred at 50.degree. for 2 hours, the solvent is then distilled off in vacuo and the residue is dissolved again in ethyl acetate. The organic phase is washed in each case twice with water and saturated sodium chloride solution, dried with sodium sulfate and evaporated in vacuo. After recrystallization of the residue from hexane, 1-phenyl-1,2-propanedione 1-E-[(2-propynyl)oxime] is obtained with a melting point of 54-56.degree. C.
H1d) 1-Phenyl-1,2-propanedione 1-E-[(2-propynyl)oxime]-2-oxime
A mixture of 14.3 g of 1-phenyl-1,2-propanedione 1-E-[(2-propynyl)oxime], 10.3 g of hydroxylamine hydrochloride and 11.7 g of pyridine in 230 ml of ethanol is boiled under reflux for 1 hour and then concentrated in vacuo, and 800 ml of water are added to the residue. The product which has precipitated out is filtered off and dissolved in ethyl acetate and the solution is washed three times with water, dried with sodium sulfate and evaporated in vacuo. The residue is suspended in hexane and filtered. The title product is thus obtained with a melting point of 163-165.degree. C.
H1e) Methyl 2-[[[(1-methyl-2-phenyl-2-E-[(2-propynyl)oxyimino]ethy-lidene)amino]oxy]-methyl]-.alpha.-(methoxymethylene)-phenylacetate
A solution of 5 g of 1-phenyl-1,2-propanedione 1-E-[(2-propynyl)oxime]-2-oxime in 24 ml of N,N-dimethylformamide is added dropwise to a suspension of 1.16 g of sodium hydride (about 55% in oil) in 45 ml of N,N-dimethylformamide at room temperature and the mixture is further stirred for 10 minutes. 6.5 g of methyl 2-(bromomethyl)-.alpha.-(methoxymethylene)-phenylacetate in 24 ml of N,N-dimethylformamide are then added dropwise and the reaction mixture is further stirred at room temperature for 1 hour. Thereafter, the mixure is acidified with acetic acid and evaporated in vacuo. The residue is dissolved in ethyl acetate and the solution is washed three times with water and twice with saturated sodium chloride solution, dried with sodium sulfate and evaporated in vacuo. After recrystallization of the residue from hexane/ethyl acetate, the title compound is obtained with a melting point of 82-84.degree..
Example H2
Methyl 2-[[[(1-methyl-2-(4-fluorophenyl)-2-E-[(2-propynyl)oxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxymethylene)-phenylacetate (compound 1.44)
The title compound with a melting point of 91-93.degree. can be prepared in a manner analogous to that described in Example H1, starting from 1-(4-fluorophenyl)-2-propanone.
Example H3
Methyl 2-[[[(1-methyl-2-(4-(3-trifluoromethylphenylmethoxy)-phenyl) 2-E-[(2propynyl)oxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxymethylene)-phenylacetate (compound 1.240)
H3a) 1-(4-Hydroxyphenyl)-2-propanone
A mixture of 82 g of 1-(4-methoxyphenyl)-2-propanone, 500 ml of acetic acid and 500 ml of aqueous hydrobromic acid is boiled under reflux for 2 hours and then evaporated in vacuo. The oily residue is extracted four times with 700 ml of hexane/ether (5:2) each time, the extract is evaporated and the residue is chromatographed over silica gel using hexane/ethyl acetate (3:1). 1-(4-Hydroxyphenyl)-2-propanone is thus obtained with a melting point of 40-41.degree..
H3b) 1-[4-(3-Trifluoromethylphenylmethoxy)-phenyl]-2-propanone
A mixture of 5.8 g of 1-(4-hydroxyphenyl)-2-propanone, 61.6 g of potassium carbonate, 72.3 g of 1-(chloromethyl)-3-(trifluoromethyl)-benzene, and 1 g of potassium iodide in 800 ml of acetone is boiled under reflux for 5 hours. Thereafter, the reaction mixture is filtered and the filtrate is evaporated in vacuo. The residue is then dissolved in diethyl ether and the ethereal phase is washed three times with water, dried with sodium sulfate and evaporated. The 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-2-propanone thus obtainable is employed in the next reaction stage without further purification.
H3c) 1-[4-(3-Trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-oxime
45 g of a 30% solution of sodium methanolate in methanol are slowly added dropwise to a solution of 59.6 g of 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-2-propanone and 23.4 g of isopentyl nitrite in 300 ml of methanol such that the temperature does not exceed 20-25.degree.. The reaction mixture is then further stirred at room temperature for 1 hour and thereafter evaporated in vacuo. The residue is dissolved in 600 ml of water and the solution is acidified with 10% hydrochloric acid. The precipitate which separates out is filtered off and dissolved in ethyl acetate and the organic phase is washed twice with water, dried with sodium sulfate and evaporated. After the crude product has been suspended in hexane and filtered, 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-oxime is obtained with a melting point of 134-136.degree..
H3d) 1-[4-(3-Trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-[(2-propynyl)oxime]
A mixture of 6 g of 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-oxime, 2.4 g of 1-bromo-2-propyne, 2.6 g of potassium carbonate and 0.5 g of potassium iodide in 40 ml of acetonitrile is boiled under reflux for 1 hour and then evaporated in vacuo and the residue is dissolved in ethyl acetate. The organic phase is washed twice with water and once with saturated sodium chloride solution, dried with sodium sulfate and evaporated. The crude 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-[(2-propynyl)oxime] thus obtainable is further processed without further purification.
H3e) 1-[4-(3-Trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-[(2-propynyl)oxime]-2-oxime
A mixture of 5.9 g of 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-[(2-propynyl)oxime], 2.3 g of hydroxylamine hydrochloride and 2.6 g of pyridine in 60 ml of ethanol is boiled under reflux for 1 hour and then concentrated in vacuo, and 200 ml of water are added to the residue. The product which has precipitated out is filtered off and dissolved in ethyl acetate, and the solution is washed twice with water and once with saturated sodium chloride solution, dried with sodium sulfate and evaporated in vacuo. The residue is suspended in hexane and filtered. 1-[4-(3-Trifluoromethylphenylmethoxy)-phenyl]1,2-propanedione 1-E-[(2-propynyl)oxime]-2-oxime is thus obtained with a melting point of 114-115.degree..
H3f) Methyl 2-[[[(1-methyl-2-(4-(3-trifluoromethylphenylmethoxy)-phenyl)-2-E-[(2-propynyl)oxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxymethylene)-phenylacetate
A solution of 5.5 g of 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-[(2-propynyl)oxime]-2-oxime in 25 ml of N,N-dimethylformamide is added dropwise to a suspension of 0.7 g of sodium hydride (about 55% in oil) in 25 ml of N,N-dimethylformamide and the mixture is further stirred at room temperature for 10 minutes. 4 g of methyl 2-(bromomethyl)-.alpha.-(methoxymethylene)-phenylacetate in 15 ml of N,N-dimethylformamide are then added dropwise and the reaction mixture is further stirred at room temperature for 1 hour. Thereafter, the mixture is acidified with acetic acid and evaporated in vacuo at 50.degree.. The residue is dissolved in ethyl acetate and the solution is washed twice with water and once with saturated sodium chloride solution, dried with sodium sulfate and evaporated in vacuo. After purification by chromatography (silica gel, ethyl acetate/hexane 1:3), the title compound is obtained as a resin.
Example H4
Methyl 2-[[[(1-methyl-2-(4-(4-chlorophenoxy)-phenyl)-2-E-[(2-ethyl)oxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxymethylene)-phenylacetate (compound 1.366)
H4a) 1-[4-(4-Chlorophenoxy)-phenyl]-1,2-propanedione 1-E-oxime
16.7 g of a 30% solution of sodium methylate in methanol are added dropwise to a solution of 22.5 g of 1-[4-(4-chlorophenoxy)-phenyl]-2-propanone and 10.3 g of isopentyl nitrite in 120 ml of methanol at 20-25.degree., while cooling. The reaction mixture is then further stirred at room temperature for 1 hour. After the solution has been concentrated in vacuo, the residue is dissolved in 300 ml of water and the solution is acidified with 10% hydrochloric acid, the product which precipitates out is filtered off and dissolved in ethyl acetate and the organic phase is washed twice with water, dried with sodium sulfate and evaporated in vacuo. The residue is stirred up in hexane and filtered. The title product is thus obtained with a melting point of 154-155.degree. C.
H4b) 1-[4-(4-Chlorophenoxy)-phenyl]-1,2-propanedione 1-E-[(2-ethyl)oxime]
A mixture of 6 g of) 1-[4-(4-Chlorophenoxy)-phenyl]-1,2-propanedione 1-E-oxime, 3.3 g of ethyl bromide, 3.5 g of potassium carbonate and 0.5 g of potassium iodide in 30 ml of acetonitrile is stirred at 50.degree. for 2 hours, the solvent is then distilled off in vacuo and the residue is dissolved again in ethyl acetate. The organic phase is washed in each case twice with water and saturated sodium chloride solution, dried with sodium sulfate and evaporated in vacuo. After recrystallization of the residue from hexane, the title product is obtained with a melting point of 77-78.degree. C.
H4c) 1-[4-(4-Chlorophenoxy)-phenyl]-1,2-propanedione 1-E-[(2-ethyl)oxime]-2-oxime
A mixture of 5.5 g of 1-[4-(4-chlorophenoxy)-phenyl]-1,2-propanedione 1-E-[(2-ethyl)oxime], 2.4 g of hydroxylamine hydrochloride and 2.7 9 of pyridine in 50 ml of ethanol is boiled under reflux for 1 hour and then concentrated in vacuo, and 800 ml of water are added to the residue. The product which has precipitated out is filtered off and dissolved in ethyl acetate and the solution is washed three times with water, dried with sodium sulfate and evaporated in vacuo. The residue is suspended in hexane and filtered. The title product is thus obtained in a pure form with a melting point of 176-177.degree. C.
H4d) Methyl 2-[[[(1-methyl-2-(4-(4-chlorophenoxy)-phenyl)-2-E-[(2-ethyl)oxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxymethylene)-phenylacetate.
A solution of 4.7 g of 1-[4-(4-chlorophenoxy)-phenyl]-1,2-propanedione 1-E-[(2-propynyl)-oxime]-2-oxime in 25 ml of N,N-dimethylformamide is added dropwise to a suspension of 0.65 g of sodium hydride (about 55% in oil) in 20 ml of N,N-dimethylformamide and the mixture is further stirred at room temperature for 10 minutes. 4 g of methyl 2-(bromomethyl)-.alpha.-(methoxymethylene)-phenylacetate in 15 ml of N,N-dimethylformamide are then added dropwise and the reaction mixture is further stirred at room temperature for 1 hour. Thereafter, the mixture is acidified with acetic acid and evaporated in vacuo at 50.degree.. The residue is dissolved in ethyl acetate and the solution is washed twice with water and once with saturated sodium chloride solution, dried with sodium sulfate and evaporated in vacuo. After purification by flash chromatography (silica gel, ethyl acetate/hexane 1:3), the title compound is obtained with a melting point of 87-89.degree. C.
Example H5
Methyl 2-[[[(1-methyl-2-(4-(4-chlorophenoxy)-phenyl)-2-E-[(2-ethyl)oxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxyimino)-phenylacetate (compound 2.366)
The title compound with a melting point of 90 to 93.degree. C. is obtained in a manner analogous to that described in Example H4 from 1-[4-(4-chlorophenoxy)-phenyl]-1,2-propanedione 1-E-[(2-propynyl)oxime]-2-oxime and methyl 2-(bromomethyl)-.alpha.-(methoxyimino)-phenylacetate.
Example H6
2-[[[(1-Methyl-2-(4-(4-chlorophenoxy)-phenyl)-2-E-[(2-ethyl)oxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxyimino)-phenylacetic acid methylamide (compound 3.366)
13,3 g of methyl 2-[[[(1-methyl-2-(4-(4-chlorophenoxy)-phenyl)-2-E-[(2-ethyl)oxyimino]ethyliene)amino]oxy]methyl]-.alpha.-(methoxyimino)-phenylacetate are left to stand together with 80 ml of dimethylformamide and 9.2 ml of an 8 molar solution of methylamine in ethanol at room temperature for two days. The mixture is concentrated at 50.degree. C., n-hexane is added and the mixture is cooled to room temperature and filtered. The residue is dried under a high vacuum. The title compound is obtained with a melting point of 126-129.degree. C.
Example H7
The other compounds listed in Tables 1 to 3 can also be prepared in a manner analogous to that described in Examples H1 to H6. In the "physical data" column of the tables, the temperatures stated in each case designate the melting point of the compound in question. c.propyl is cyclopropyl.
TABLE 1______________________________________ Compounds of the general formula______________________________________ I.1 ##STR9##______________________________________
in which X is CH and Y is oxygen and the combination of substituents R.sub.2, (R.sub.5).sub.n and A--R.sub.7 for a compound in each case corresponds to a line in Table A. The compound numbers of the following table correspond to the particular numbers in Table A.
______________________________________Compound No. Phys. Data( Melting point .degree. C.)______________________________________1.14 75-77.degree. 1.16 82-84.degree. 1.22 111-113.degree. 1.42 Resin 1.44 91-93.degree. 1.50 Resin 1.70 Resin 1.72 Resin 1.78 Resin 1.225 102-113.degree. 1.226 81-83.degree. 1.227 Resin 1.233 Resin 1.234 73-75.degree. 1.238 Resin 1.240 Resin 1.241 Resin 1.242 Resin 1.244 Resin 1.245 Resin 1.294 Resin 1.296 112-114.degree. 1.366 87-89.degree.______________________________________
TABLE 2______________________________________Compounds of the general formula I.1, in which X is nitrogen and Y is oxygen and the combination of substituents R.sub.2, (R.sub.5).sub.n andA-R.sub.7 for a compound in each case corresponds to a line in Table A. Compound No. Melting point (.degree. C.)______________________________________2.198 75-77 2.254 80-82 2.309 106-108 2.310 102-104 2.366 90-93______________________________________
TABLE 3______________________________________Compounds of the general formula I.1, in which X is nitrogen and Y is NH and the combination of substituents R.sub.2, (R.sub.5).sub.n and A-R.sub.7 for a compound in each case corresponds to a line in Table A. Compound No. Melting point (.degree. C.)______________________________________3.198 75-77 3.254 112-114 3.309 89-91 3.310 88-90 3.366 126-129______________________________________
TABLE A______________________________________Compound No. R.sub.2 (R.sub.5).sub.n A-R.sub.7______________________________________ 1 CH.sub.3 H CH.sub.3 2 CH.sub.3 H C.sub.2 H.sub.5 3 CH.sub.3 H n-C.sub.3 H.sub.7 4 CH.sub.3 H i-C.sub.3 H.sub.7 5 CH.sub.3 H n-C.sub.4 H.sub.9 6 CH.sub.3 H n-C.sub.6 H.sub.13 7 CH.sub.3 H CH.sub.2 F 8 CH.sub.3 H CHF.sub.2 9 CH.sub.3 H CH.sub.2 CF.sub.3 10 CH.sub.3 H CH.sub.2 CH=CH.sub.2 11 CH.sub.3 H CH.sub.2 CH=CHCH.sub.3 12 CH.sub.3 H CH.sub.2 CH=C(CH.sub.3).sub.2 13 CH.sub.3 H CH.sub.2 CH=CHCl 14 CH.sub.3 H CH.sub.2 CH=CCl.sub.2 15 CH.sub.3 H CH.sub.2 C(CH.sub.3)=CH.sub.2 16 CH.sub.3 H CH.sub.2 C=CH 17 CH.sub.3 H CH.sub.2 Si(CH.sub.3).sub.3 18 CH.sub.3 H CH.sub.2 -c.propyl-2,2-Cl.sub.2 19 CH.sub.3 H CH.sub.2 CN 20 CH.sub.3 H CH.sub.2 COOC.sub.2 H.sub.5 21 CH.sub.3 H CH(CH.sub.3)COOC.sub.2 H.sub.5 22 CH.sub.3 H CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 23 CH.sub.3 H CH.sub.2 C.sub.6 H.sub.4 -4-F 24 CH.sub.3 H CH.sub.2 C.sub.6 H.sub.4 -3-F 25 CH.sub.3 H CH.sub.2 C.sub.6 H.sub.4 -2-F 26 CH.sub.3 H C(=O)OC.sub.2 H.sub.5 27 CH.sub.3 H C(=O)NHCH.sub.3 28 CH.sub.3 H C(=O)C(=O)OC.sub.2 H.sub.5 29 CH.sub.3 4-F CH.sub.3 30 CH.sub.3 4-F C.sub.2 H.sub.5 31 CH.sub.3 4-F n-C.sub.3 H.sub.7 32 CH.sub.3 4-F i-C.sub.3 H.sub.7 33 CH.sub.3 4-F n-C.sub.4 H.sub.9 34 CH.sub.3 4-F n-C.sub.6 H.sub.13 35 CH.sub.3 4-F CH.sub.2 F 36 CH.sub.3 4-F CHF.sub.2 37 CH.sub.3 4-F CH.sub.2 CF.sub.3 38 CH.sub.3 4-F CH.sub.2 CH=CH.sub.2 39 CH.sub.3 4-F CH.sub.2 CH=CHCH.sub.3 40 CH.sub.3 4-F CH.sub.2 CH=C(CH.sub.3).sub.2 41 CH.sub.3 4-F CH.sub.2 CH=CHCl 42 CH.sub.3 4-F CH.sub.2 CH=CCl.sub.2 43 CH.sub.3 4-F CH.sub.2 C(CH.sub.3)=CH.sub.2 44 CH.sub.3 4-F CH.sub.2 C=CH 45 CH.sub.3 4-F CH.sub.2 Si(CH.sub.3).sub.3 46 CH.sub.3 4-F CH.sub.2 -c.propyl-2,2-Cl.sub.2 47 CH.sub.3 4-F CH.sub.2 CN 48 CH.sub.3 4-F CH.sub.2 COOC.sub.2 H.sub.5 49 CH.sub.3 4-F CH(CH.sub.3)COOC.sub.2 H.sub.5 50 CH.sub.3 4-F CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 51 CH.sub.3 4-F CH.sub.2 C.sub.6 H.sub.4 -4-F 52 CH.sub.3 4-F CH.sub.2 C.sub.6 H.sub.4 -3-F 53 CH.sub.3 4-F CH.sub.2 C.sub.6 H.sub.4 -2-F 54 CH.sub.3 4-F C(=O)OC.sub.2 H.sub.5 55 CH.sub.3 4-F C(=O)NHCH.sub.3 56 CH.sub.3 4-F C(=O)C(=O)OC.sub.2 H.sub.5 57 CH.sub.3 4-OCH.sub.3 CH.sub.3 58 CH.sub.3 4-OCH.sub.3 C.sub.2 H.sub.5 59 CH.sub.3 4-OCH.sub.3 n-C.sub.3 H.sub.7 60 CH.sub.3 4-OCH.sub.3 i-C.sub.3 H.sub.7 61 CH.sub.3 4-OCH.sub.3 n-C.sub.4 H.sub.9 62 CH.sub.3 4-OCH.sub.3 n-C.sub.6 H.sub.13 63 CH.sub.3 4-OCH.sub.3 CH.sub.2 F 64 CH.sub.3 4-OCH.sub.3 CHF.sub.2 65 CH.sub.3 4-OCH.sub.3 CH.sub.2 CF.sub.3 66 CH.sub.3 4-OCH.sub.3 CH.sub.2 CH=CH.sub.2 67 CH.sub.3 4-OCH.sub.3 CH.sub.2 CH=CHCH.sub.3 68 CH.sub.3 4-OCH.sub.3 CH.sub.2 CH=C(CH.sub.3).sub.2 69 CH.sub.3 4-OCH.sub.3 CH.sub.2 CH=CHCl 70 CH.sub.3 4-OCH.sub.3 CH.sub.2 CH=CCl.sub.2 71 CH.sub.3 4-OCH.sub.3 CH.sub.2 C(CH.sub.3)=CH.sub.2 72 CH.sub.3 4-OCH.sub.3 CH.sub.2 C=CH 73 CH.sub.3 4-OCH.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 74 CH.sub.3 4-OCH.sub.3 CH.sub.2 -c. propyl-2,2-Cl.sub.2 75 CH.sub.3 4-OCH.sub.3 CH.sub.2 CN 76 CH.sub.3 4-OCH.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 77 CH.sub.3 4-OCH.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 78 CH.sub.3 4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 79 CH.sub.3 4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 80 CH.sub.3 4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 81 CH.sub.3 4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 82 CH.sub.3 4-OCH.sub.3 C(=O)OC.sub.2 H.sub.5 83 CH.sub.3 4-OCH.sub.3 C(=O)NHCH.sub.3 84 CH.sub.3 4-OCH.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 85 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.3 86 CH.sub.3 4-OC.sub.2 H.sub.5 C.sub.2 H.sub.5 87 CH.sub.3 4-OC.sub.2 H.sub.5 n-C.sub.3 H.sub.7 88 CH.sub.3 4-OC.sub.2 H.sub.5 i-C.sub.3 H.sub.7 89 CH.sub.3 4-OC.sub.2 H.sub.5 n-C.sub.4 H.sub.9 90 CH.sub.3 4-OC.sub.2 H.sub.5 n-C.sub.6 H.sub.13 91 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 F 92 CH.sub.3 4-OC.sub.2 H.sub.5 CHF.sub.2 93 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 CF.sub.3 94 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 CH=CH.sub.2 95 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 CH=CHCH.sub.3 96 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 CH=C(CH.sub.3).sub.2 97 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 CH=CHCl 98 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 CH=CCl.sub.2 99 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 C(CH.sub.3)=CH.sub.2 100 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 C=CH 101 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 Si(CH.sub.3).sub.3 102 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 -c.propyl-2,2-Cl.sub.2 103 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 CN 104 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 COOC.sub.2 H.sub.5 105 CH.sub.3 4-OC.sub.2 H.sub.5 CH(CH.sub.3)COOC.sub.2 H.sub.5 106 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 107 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 C.sub.6 H.sub.4 -4-F 108 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 C.sub.6 H.sub.4 -3-F 109 CH.sub.3 4-OC.sub.2 H.sub.5 CH.sub.2 C.sub.6 H.sub.4 -2-F 110 CH.sub.3 4-OC.sub.2 H.sub.5 C(=O)OC.sub.2 H.sub.5 111 CH.sub.3 4-OC.sub.2 H.sub.5 C(=O)NHCH.sub.3 112 CH.sub.3 4-OC.sub.2 H.sub.5 C(=O)C(=O)OC.sub.2 H.sub.5 113 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.3 114 CH.sub.3 4-O-n-C.sub.3 H.sub.7 C.sub.2 H.sub.5 115 CH.sub.3 4-O-n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.7 116 CH.sub.3 4-O-n-C.sub.3 H.sub.7 i-C.sub.3 H.sub.7 117 CH.sub.3 4-O-n-C.sub.3 H.sub.7 n-C.sub.4 H.sub.9 118 CH.sub.3 4-O-n-C.sub.3 H.sub.7 n-C.sub.6 H.sub.13 119 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 F 120 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CHF.sub.2 121 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 CF.sub.3 122 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 CH=CH.sub.2 123 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 CH=CHCH.sub.3 124 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 CH=C(CH.sub.3).sub.2 125 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 CH=CHCl 126 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 CH=CCl.sub.2 127 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 C(CH.sub.3)=CH.sub.2 128 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 C=CH 129 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 Si(CH.sub.3).sub.3 130 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 -c.propyl-2,2-Cl.sub.2 131 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 CN 132 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 COOC.sub.2 H.sub.5 133 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH(CH.sub.3)COOC.sub.2 H.sub.5 134 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 135 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 C.sub.6 H.sub.4 -4-F 136 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 C.sub.6 H.sub.4 -3-F 137 CH.sub.3 4-O-n-C.sub.3 H.sub.7 CH.sub.2 C.sub.6 H.sub.4 -2-F 138 CH.sub.3 4-O-n-C.sub.3 H.sub.7 C(=O)OC.sub.2 H.sub.5 139 CH.sub.3 4-O-n-C.sub.3 H.sub.7 C(=O)NHCH.sub.3 140 CH.sub.3 4-O-n-C.sub.3 H.sub.7 C(=O)C(=O)OC.sub.2 H.sub.5 141 CH.sub.3 2-CH.sub.3 CH.sub.3 142 CH.sub.3 2-CH.sub.3 C.sub.2 H.sub.5 143 CH.sub.3 2-CH.sub.3 n-C.sub.3 H.sub.7 144 CH.sub.3 2-CH.sub.3 i-C.sub.3 H.sub.7 145 CH.sub.3 2-CH.sub.3 n-C.sub.4 H.sub.9 146 CH.sub.3 2-CH.sub.3 n-C.sub.6 H.sub.13 147 CH.sub.3 2-CH.sub.3 CH.sub.2 F 148 CH.sub.3 2-CH.sub.3 CHF.sub.2 149 CH.sub.3 2-CH.sub.3 CH.sub.2 CF.sub.3 150 CH.sub.3 2-CH.sub.3 CH.sub.2 CH=CH.sub.2 151 CH.sub.3 2-CH.sub.3 CH.sub.2 CH=CHCH.sub.3 152 CH.sub.3 2-CH.sub.3 CH.sub.2 CH=C(CH.sub.3).sub.2 153 CH.sub.3 2-CH.sub.3 CH.sub.2 CH=CHCl 154 CH.sub.3 2-CH.sub.3 CH.sub.2 CH=CCl.sub.2 155 CH.sub.3 2-CH.sub.3 CH.sub.2 C(CH.sub.3)=CH.sub.2 156 CH.sub.3 2-CH.sub.3 CH.sub.2 C=CH 157 CH.sub.3 2-CH.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 158 CH.sub.3 2-CH.sub.3 CH.sub.2 -c.propyl-2,2-Cl.sub.2 159 CH.sub.3 2-CH.sub.3 CH.sub.2 CN 160 CH.sub.3 2-CH.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 161 CH.sub.3 2-CH.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 162 CH.sub.3 2-CH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 163 CH.sub.3 2-CH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 164 CH.sub.3 2-CH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 165 CH.sub.3 2-CH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 166 CH.sub.3 2-CH.sub.3 C(=O)OC.sub.2 H.sub.5 167 CH.sub.3 2-CH.sub.3 C(=O)NHCH.sub.3 168 CH.sub.3 2-CH.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 169 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.3 170 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 C.sub.2 H.sub.5 171 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 n-C.sub.3 H.sub.7 172 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 i-C.sub.3 H.sub.7 173 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 n-C.sub.4 H.sub.9 174 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 n-C.sub.6 H.sub.13 175 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 F 176 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CHF.sub.2 177 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 CF.sub.3 178 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 CH=CH.sub.2 179 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub. 3 CH.sub.2 CH=CHCH.sub.3 180 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 CH=C(CH.sub.3).sub. 2 181 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 CH=CHCl 182 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 CH=CCl.sub.2 183 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub. 3 CH.sub.2 C(CH.sub.3)=CH.sub.2 184 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 C=CH 185 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 Si(CH.sub.3).sub.3 186 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 -c.propyl-2,2-Cl.su b.2 187 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 CN 188 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 COOC.sub.2 H.sub.5 189 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 190 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 191 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 192 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 193 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 194 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 C(=O)OC.sub.2 H.sub.5 195 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub. 3 C(=O)NHCH.sub.3 196 CH.sub.3 4-OCH.sub.2 Si(CH.sub.3).sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 197 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.3 198 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 C.sub.2 H.sub.5 199 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 n-C.sub.3 H.sub.7 200 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 i-C.sub.3 H.sub.7 201 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 n-C.sub.4 H.sub.9 202 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 n-C.sub.6 H.sub.13 203 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 F 204 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CHF.sub.2 205 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CF.sub.3 206 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=CH.sub.2 207 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=CHCH.su b.3 208 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=C(CH.su b.3).sub.2 209 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=CHCl 210 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=CCl.sub.2 211 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C(CH.sub.3 )=CH.sub.2 212 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C=CH 213 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 214 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 -c.propyl-2,2-Cl.sub.2 215 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CN 216 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 217 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 218 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 219 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 220 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 221 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 222 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 C(=O)OC.sub.2 H.sub.5 223 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 C(=O)NHCH.sub.3 224 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-CF.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 225 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.3 226 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 C.sub.2 H.sub.5 227 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 n-C.sub.3 H.sub.7 228 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 i-C.sub.3 H.sub.7 229 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 n-C.sub.4 H.sub.9 230 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 n-C.sub.6 H.sub.13 231 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 F 232 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CHF.sub.2 233 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CF.sub.3 234 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CH.sub.2 235 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CHCH.su b.3 236 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=C(CH.su b.3).sub.2 237 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CHCl 238 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CCl.sub.2 239 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C(CH.sub.3 )=CH.sub.2 240 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C=CH 241 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 242 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 -c.propyl-2,2-Cl.sub.2 243 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CN 244 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 245 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 246 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 247 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 248 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 249 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 250 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 C(=O)OC.sub.2 H.sub.5 251 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 C(=O)NHCH.sub.3 252 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 253 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.3 254 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 C.sub.2 H.sub.5 255 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF3 n-C.sub.3 H.sub.7 256 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 i-C.sub.3 H.sub.7 257 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 n-C.sub.4 H.sub.9 258 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 n-C.sub.6 H.sub.13 259 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 F 260 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CHF.sub.2 261 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CF.sub.3 262 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=CH.sub.2 263 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=CHCH.su b.3 264 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=C(CH.su b.3).sub.2 265 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=CHCl 266 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=CCl.sub.2 267 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C(CH.sub.3 )=CH.sub.2 268 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C=CH 269 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 270 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 -c.propyl-2,2-Cl.sub.2 271 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CN 272 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 273 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 274 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 275 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 276 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 277 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 278 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 C(=O)OC.sub.2 H.sub.5 279 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 C(=O)NHCH.sub.3 280 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -2-CF.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 281 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.3 282 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F C.sub.2 H.sub.5 283 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F n-C.sub.3 H.sub.7 284 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F i-C.sub.3 H.sub.7 285 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F n-C.sub.4 H.sub.9 286 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F n-C.sub.6 H.sub.13 287 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 F 288 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CHF.sub.2 289 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 CF.sub.3 290 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 CH=CH.sub.2 291 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 CH=CHCH.sub.3 292 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 CH=C(CH.sub.3).sub.2 293 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 CH=CHCl 294 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 CH=CCl.sub.2 295 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 C(CH.sub.3)=CH.sub.2 296 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 C=CH 297 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 Si(CH.sub.3).sub. 3 298 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 -c.propyl-2,2-Cl. sub.2 299 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 CN 300 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 COOC.sub.2 H.sub.5 301 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH(CH.sub.3)COOC.sub.2 H.sub.5 302 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 303 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -4-F 304 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -3-F 305 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -2-F 306 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F C(=O)OC.sub.2 H.sub.5 307 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F C(=O)NHCH.sub.3 308 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-F C(=O)C(=O)OC.sub.2 H.sub.5 309 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.3 310 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 C.sub.2 H.sub.5 311 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 n-C.sub.3 H.sub.7 312 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 i-C.sub.3 H.sub.7 313 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 n-C.sub.4 H.sub.9 314 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 n-C.sub.6 H.sub.13 315 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 F 316 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CHF.sub.2 317 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 CF.sub.3 318 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 CH=CH.sub.2 319 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 CH=CHCH.sub.3 320 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 CH=C(CH.sub.3).sub.2 321 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 CH=CHCl 322 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 CH=CCl.sub.2 323 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 C(CH.sub.3)=CH.sub.2 324 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 C=CH 325 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 326 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 -c.propyl-2,2-Cl.sub.2 327 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 CN 328 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 329 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 330 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 331 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 332 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 333 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 334 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 C(=O)OC.sub.2 H.sub.5 335 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 C(=O)NHCH.sub.3 336 CH.sub.3 4-OC.sub.6 H.sub.4 3-CF.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 337 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.3 338 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 C.sub.2 H.sub.5 339 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 n-C.sub.3 H.sub.7 340 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 i-C.sub.3 H.sub.7 341 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 n-C.sub.4 H.sub.9 342 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 n-C.sub.6 H.sub.13 343 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 F 344 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CHF.sub.2 345 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CF.sub.3 346 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CH.sub.2 347 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CHCH.sub.3 348 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=C(CH.sub.3).sub.2 349 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CHCl 350 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CH=CCl.sub.2 351 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C(CH.sub.3)=CH.sub.2 352 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C=CH 353 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 354 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 -c.propyl-2,2-Cl.sub.2 355 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 CN 356 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 357 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH(CH.sub.3) COOC.sub.2 H.sub.5 358 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 359 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 360 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 361 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 362 C.sub.2 H.sub.5 4-OC.sub.6 H.sub.4 -3-CF.sub.3 C(=O)OC.sub.2 H.sub.5 363 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 C(=O)NHCH.su b.3 364 C.sub.2 H.sub.5 4-OCH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 C(=O)C(=O)OC .sub.2 H.sub.5 365 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.3 366 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl C.sub.2 H.sub.5 367 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl n-C.sub.3 H.sub.7 368 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl i-C.sub.3 H.sub.7 369 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl n-C.sub.4 H.sub.9 370 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl n-C.sub.6 H.sub.13 371 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 F 372 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CHF.sub.2 373 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 CF.sub.3 374 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CH.sub.2 375 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CHCH.sub.3 376 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=C(CH.sub.3).sub.2 377 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CHCl 378 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CCl.sub.2 379 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 C(CH.sub.3)=CH.sub.2 380 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 C=CH 381 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 Si(CH.sub.3).sub.3 382 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 -c.propyl-2,2-Cl.sub.2 383 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 CN 384 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 COOC.sub.2 H.sub.5 385 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH(CH.sub.3)COOC.sub.2 H.sub.5 386 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub .3 387 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -4-F 388 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -3-F 389 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -2-F 390 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl C(=O)OC.sub.2 H.sub.5 391 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl C(=O)NHCH.sub.3 392 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Cl C(=O)C(=O)OC.sub.2 H.sub.5 393 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.3 394 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl C.sub.2 H.sub.5 395 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl n-C.sub.3 H.sub.7 396 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl i-C.sub.3 H.sub.7 397 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl n-C.sub.4 H.sub.9 398 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl n-C.sub.6 H.sub.13 399 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 F 400 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CHF.sub.2 401 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 CF.sub.3 402 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 CH=CH.sub.2 403 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 CH=CHCH.sub.3 404 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 CH=C(CH.sub.3).sub.2 405 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 CH=CHCl 406 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 CH=CCl.sub.2 407 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 C(CH.sub.3)=CH.sub.2 408 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 C=CH 409 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 Si(CH.sub.3).sub.3 410 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 -c.propyl-2,2-Cl.sub.2 411 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 CN 412 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 COOC.sub.2 H.sub.5 413 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH(CH.sub.3)COOC.sub.2 H.sub.5 414 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub .3 415 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 C.sub.6 H.sub.4 -4-F 416 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 C.sub.6 H.sub.4 -3-F 417 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl CH.sub.2 C.sub.6 H.sub.4 -2-F 418 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl C(=O)OC.sub.2 H.sub.5 419 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl C(=O)NHCH.sub.3 420 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Cl C(=O)C(=O)OC.sub.2 H.sub.5 421 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.3 422 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl C.sub.2 H.sub.5 423 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl n-C.sub.3 H.sub.7 424 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl i-C.sub.3 H.sub.7 425 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl n-C.sub.4 H.sub.9 426 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl n-C.sub.6 H.sub.13 427 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 F 428 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CHF.sub.2 429 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 CF.sub.3 430 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 CH=CH.sub.2 431 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 CH=CHCH.sub.3 432 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 CH=C(CH.sub.3).sub.2 433 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 CH=CHCl 434 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 CH=CCl.sub.2 435 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 C(CH.sub.3)=CH.sub.2 436 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 C=CH 437 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 Si(CH.sub.3).sub.3 438 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 -c.propyl-2,2-Cl.sub.2 439 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 CN 440 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 COOC.sub.2 H.sub.5 441 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH(CH.sub.3)COOC.sub.2 H.sub.5 442 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub .3 443 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 C.sub.6 H.sub.4 -4-F 444 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 C.sub.6 H.sub.4 -3-F 445 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl CH.sub.2 C.sub.6 H.sub.4 -2-F 446 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl C(=O)OC.sub.2 H.sub.5 447 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl C(=O)NHCH.sub.3 448 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Cl C(=O)C(=O)OC.sub.2 H.sub.5 449 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.3 450 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F C.sub.2 H.sub.5 451 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F n-C.sub.3 H.sub.7 452 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F i-C.sub.3 H.sub.7 453 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F n-C.sub.4 H.sub.9 454 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F n-C.sub.6 H.sub.13 455 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 F 456 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CHF.sub.2 457 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 CF.sub.3 458 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 CH=CH.sub.2 459 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 CH=CHCH.sub.3 460 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 CH=C(CH.sub.3).sub.2 461 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 CH=CHCl 462 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 CH=CCl.sub.2 463 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 C(CH.sub.3)=CH.sub.2 464 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 C=CH 465 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 Si(CH.sub.3).sub.3 466 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 -c.propyl-2,2-Cl.sub.2 467 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 CN 468 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 COOC.sub.2 H.sub.5 469 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH(CH.sub.3)COOC.sub.2 H.sub.5 470 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub. 3 471 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -4-F 472 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -3-F 473 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F CH.sub.2 C.sub.6 H.sub.4 -2-F 474 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F C(=O)OC.sub.2 H.sub.5 475 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F C(=O)NHCH.sub.3 476 CH.sub.3 4-OC.sub.6 H.sub.4 -4-F C(=O)C(=O)OC.sub.2 H.sub.5 477 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.3 478 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F C.sub.2 H.sub.5 479 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F n-C.sub.3 H.sub.7 480 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F i-C.sub.3 H.sub.7 481 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F n-C.sub.4 H.sub.9 482 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F n-C.sub.6 H.sub.13 483 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 F 484 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CHF.sub.2 485 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 CF.sub.3 486 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 CH=CH.sub.2 487 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 CH=CHCH.sub.3 488 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 CH=C(CH.sub.3).sub.2 489 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 CH=CHCl 490 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 CH=CCl.sub.2 491 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 C(CH.sub.3)=CH.sub.2 492 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 C=CH 493 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 Si(CH.sub.3).sub.3 494 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 -c.propyl-2,2-Cl.sub.2 495 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 CN 496 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 COOC.sub.2 H.sub.5 497 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH(CH.sub.3)COOC.sub.2 H.sub.5 498 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub. 3 499 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 C.sub.6 H.sub.4 -4-F 500 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 C.sub.6 H.sub.4 -3-F 501 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F CH.sub.2 C.sub.6 H.sub.4 -2-F 502 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F C(=O)OC.sub.2 H.sub.5 503 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F C(=O)NHCH.sub.3 504 CH.sub.3 4-OC.sub.6 H.sub.4 -3-F C(=O)C(=O)OC.sub.2 H.sub.5 505 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.3 506 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F C.sub.2 H.sub.5 507 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F n-C.sub.3 H.sub.7 508 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F i-C.sub.3 H.sub.7 509 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F n-C.sub.4 H.sub.9 510 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F n-C.sub.6 H.sub.13 511 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 F 512 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CHF.sub.2 513 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 CF.sub.3 514 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 CH=CH.sub.2 515 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 CH=CHCH.sub.3 516 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 CH=C(CH.sub.3).sub.2 517 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 CH=CHCl 518 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 CH=CCl.sub.2 519 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 C(CH.sub.3)=CH.sub.2 520 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 C=CH 521 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 Si(CH.sub.3).sub.3 522 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 -c.propyl-2,2-Cl.sub.2 523 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 CN 524 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 COOC.sub.2 H.sub.5 525 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH(CH.sub.3)COOC.sub.2 H.sub.5 526 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub. 3 527 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 C.sub.6 H.sub.4 -4-F 528 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 C.sub.6 H.sub.4 -3-F 529 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F CH.sub.2 C.sub.6 H.sub.4 -2-F 530 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F C(=O)OC.sub.2 H.sub.5 531 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F C(=O)NHCH.sub.3 532 CH.sub.3 4-OC.sub.6 H.sub.4 -2-F C(=O)C(=O)OC.sub.2 H.sub.5 533 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.3 534 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br C.sub.2 H.sub.5 535 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br n-C.sub.3 H.sub.7 536 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br i-C.sub.3 H.sub.7 537 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br n-C.sub.4 H.sub.9 538 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br n-C.sub.6 H.sub.13 539 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 F 540 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CHF.sub.2 541 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 CF.sub.3 542 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 CH=CH.sub.2 543 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 CH=CHCH.sub.3 544 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 CH=C(CH.sub.3).sub.2 545 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 CH=CHCl 546 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 CH=CCl.sub.2 547 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 C(CH.sub.3)=CH.sub.2 548 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 C=CH 549 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 Si(CH.sub.3).sub.3 550 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 -c.propyl-2,2-Cl.sub.2 551 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 CN 552 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 COOC.sub.2 H.sub.5 553 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH(CH.sub.3)COOC.sub.2 H.sub.5 554 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub .3 555 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 C.sub.6 H.sub.4 -4-F 556 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 C.sub.6 H.sub.4 -3-F 557 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br CH.sub.2 C.sub.6 H.sub.4 -2-F 558 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br C(=O)OC.sub.2 H.sub.5 559 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br C(=O)NHCH.sub.3 560 CH.sub.3 4-OC.sub.6 H.sub.4 -4-Br C(=O)C(=O)OC.sub.2 H.sub.5 561 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.3 562 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br C.sub.2 H.sub.5 563 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br n-C.sub.3 H.sub.7 564 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br i-C.sub.3 H.sub.7 565 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br n-C.sub.4 H.sub.9 566 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br n-C.sub.6 H.sub.13 567 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 F 568 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CHF.sub.2 569 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 CF.sub.3 570 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 CH=CH.sub.2 571 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 CH=CHCH.sub.3 572 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 CH=C(CH.sub.3).sub.2 573 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 CH=CHCl 574 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 CH=CCl.sub.2 575 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 C(CH.sub.3)=CH.sub.2 576 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 C=CH 577 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 Si(CH.sub.3).sub.3 578 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 -c.propyl-2,2-Cl.sub.2 579 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 CN 580 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 COOC.sub.2 H.sub.5 581 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH(CH.sub.3)COOC.sub.2 H.sub.5 582 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub .3 583 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 C.sub.6 H.sub.4 -4-F 584 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 C.sub.6 H.sub.4 -3-F 585 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br CH.sub.2 C.sub.6 H.sub.4 -2-F 586 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br C(=O)OC.sub.2 H.sub.5 587 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br C(=O)NHCH.sub.3 588 CH.sub.3 4-OC.sub.6 H.sub.4 -3-Br C(=O)C(=O)OC.sub.2 H.sub.5 589 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.3 590 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br C.sub.2 H.sub.5 591 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br n-C.sub.3 H.sub.7 592 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br i-C.sub.3 H.sub.7 593 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br n-C.sub.4 H.sub.9 594 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br n-C.sub.6 H.sub.13 595 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 F 596 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CHF.sub.2 597 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 CF.sub.3 598 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 CH=CH.sub.2 599 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 CH=CHCH.sub.3 600 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 CH=C(CH.sub.3).sub.2 601 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 CH=CHCl 602 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 CH=CCl.sub.2 603 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 C(CH.sub.3)=CH.sub.2 604 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 C=CH 605 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 Si(CH.sub.3).sub.3 606 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 -c.propyl-2,2-Cl.sub.2 607 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 CN 608 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 COOC.sub.2 H.sub.5 609 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH(CH.sub.3)COOC.sub.2 H.sub.5 610 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub .3 611 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 C.sub.6 H.sub.4 -4-F 612 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 C.sub.6 H.sub.4 -3-F 613 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br CH.sub.2 C.sub.6 H.sub.4 -2-F 614 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br C(=O)OC.sub.2 H.sub.5 615 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br C(=O)NHCH.sub.3 616 CH.sub.3 4-OC.sub.6 H.sub.4 -2-Br C(=O)C(=O)OC.sub.2 H.sub.5 617 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.su b.2 CH.sub.3 618 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 C.sub.2 H.sub.5 619 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 n-C.sub.3 H.sub.7 620 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.su b.2 i-C.sub.3 H.sub.7 621 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 n-C.sub.4 H.sub.9 622 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.su b.2 n-C.sub.6 H.sub.13 623 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 F 624 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CHF.sub.2 625 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 CF.sub.3 626 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.su b.2 CH.sub.2 CH=CH.sub.2 627 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 CH=CHCH.sub.3 628 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.su b.2 CH.sub.2 CH=C(CH.sub.3).sub.2 629 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 CH=CHCl 630 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 CH=CCl.sub.2 631 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.su b.2 CH.sub.2 C(CH.sub.3)=CH.sub.2 632 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 C=CH 633 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 Si(CH.sub.3).sub. 3 634 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 -c.propyl-2,2-Cl. sub.2 635 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 CN 636 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 637 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH(CH.sub.3)COOC.sub.2 H.sub.5 638 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 639 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -4-F 640 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -3-F 641 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -2-F 642 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 C(=O)OC.sub.2 H.sub.5 643 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.su b.2 C(=O)NHCH.sub.3 644 CH.sub.3 4-OC.sub.6 H.sub.3 -2,4-Cl.sub.2 C(=O)C(=O)OC.sub.2 H.sub.5 645 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.3 646 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 C.sub.2 H.sub.5 647 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 n-C.sub.3 H.sub.7 648 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.su b.2 i-C.sub.3 H.sub.7 649 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 n-C.sub.4 H.sub.9 650 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.su b.2 n-C.sub.6 H.sub.13 651 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 F 652 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CHF.sub.2 653 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CF.sub.3 654 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.su b.2 CH.sub.2 CH=CH.sub.2 655 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=CHCH.sub.3 656 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.su b.2 CH.sub.2 CH=C(CH.sub.3).sub.2 657 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=CHCl 658 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=CCl.sub.2 659 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.su b.2 CH.sub.2 C(CH.sub.3)=CH.sub.2 660 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C=CH 661 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 Si(CH.sub.3).sub. 3 662 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 -c.propyl-2,2-Cl. sub.2 663 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CN 664 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 665 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH(CH.sub.3)COOC.sub.2 H.sub.5 666 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 667 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -4-F 668 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -3-F 669 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -2-F 670 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 C(=O)OC.sub.2 H.sub.5 671 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.su b.2 C(=O)NHCH.sub.3 672 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-Cl.sub.2 C(=O)C(=O)OC.sub.2 H.sub.5 673 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.3 674 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br C.sub.2 H.sub.5 675 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br n-C.sub.3 H.sub.7 676 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br i-C.sub.3 H.sub.7 677 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br n-C.sub.4 H.sub.9 678 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br n-C.sub.6 H.sub.13 679 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 F 680 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CHF.sub.2 681 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 CF.sub.3 682 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 CH=CH.sub.2 683 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 CH=CHCH.sub.3 684 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 CH=C(CH.sub.3).sub.2 685 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 CH=CHCl 686 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 CH=CCl.sub.2 687 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 C(CH.sub.3)=CH.sub.2 688 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 C=CH 689 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 Si(CH.sub.3).sub.3 690 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 -c.propyl-2,2-Cl.sub.2 691 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 CN 692 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 COOC.sub.2 H.sub.5 693 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH(CH.sub.3)COOC.sub.2 H.sub.5 694 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 695 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 C.sub.6 H.sub.4 -4-F 696 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 C.sub.6 H.sub.4 -3-F 697 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br CH.sub.2 C.sub.6 H.sub.4 -2-F 698 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br C(=O)OC.sub.2 H.sub.5 699 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br C(=O)NHCH.sub.3 700 CH.sub.3 4-OC.sub.6 H.sub.3 -2-Cl,4-Br C(=O)C(=O)OC.sub.2 H.sub.5 701 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) CH.sub.3 702 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) C.sub.2 H.sub.5 703 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) n-C.sub.3 H.sub.7 704 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) i-C.sub.3 H.sub.7 705 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) n-C.sub.4 H.sub.9 706 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) n-C.sub.6 H.sub.13 707 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) CH.sub.2 F 708 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CHF.sub.2 709 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 CF.sub.3 710 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) CH.sub.2 CH=CH.sub.2 711 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 CH=CHCH.sub .3 712 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 CH=C(CH.sub .3).sub.2 713 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 CH=CHCl 714 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) CH.sub.2 CH=CCl.sub.2 715 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 C(CH.sub.3) =CH.sub.2 716 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 C=CH 717 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) CH.sub.2 Si(CH.sub.3).sub.3 718 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) CH.sub.2 -c.propyl-2,2-Cl.sub.2 719 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) CH.sub.2 CN 720 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 COOC.sub.2 H.sub.5 721 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH(CH.sub.3)COOC.sub .2 H.sub.5 722 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 723 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 C.sub.6 H.sub.4 -4-F 724 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 C.sub.6 H.sub.4 -3-F 725 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) CH.sub.2 C.sub.6 H.sub.4 -2-F 726 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) C(=O)OC.sub.2 H.sub.5 727 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH.sub.2 O-) C(=O)NHCH.sub.3 728 CH.sub.3 4-OC.sub.6 H.sub.3 -3,4-(-CH. sub.2 O-) C(=O)C(=O)OC.sub.2 H.sub.5 729 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub .3 CH.sub.3 730 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 C.sub.2 H.sub.5 731 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 n-C.sub.3 H.sub.7 732 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 i-C.sub.3 H.sub.7 733 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 n-C.sub.4 H.sub.9 734 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 n-C.sub.6 H.sub.13 735 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub .3 CH.sub.2 F 736 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CHF.sub.2 737 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 CF.sub.3 738 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 CH=CH.sub.2 739 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub .3 CH.sub.2 CH=CHCH.sub.3 740 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 CH=C(CH.sub.3).sub .2 741 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 CH=CHCl 742 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 CH=CCl.sub.2 743 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub .3 CH.sub.2 C(CH.sub.3)=CH.sub.2 744 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 C=CH 745 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 746 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 -c.propyl-2,2-Cl.s ub.2 747 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 CN 748 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 749 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 750 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 751 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 752 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 753 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 754 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 C(=O)OC.sub.2 H.sub.5 755 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub .3 C(=O)NHCH.sub.3 756 CH.sub.3 4-OC.sub.6 H.sub.4 -4-SCH.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 757 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.3 758 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 C.sub.2 H.sub.5 759 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 n-C.sub.3 H.sub.7 760 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 i-C.sub.3 H.sub.7 761 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 n-C.sub.4 H.sub.9 762 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 n-C.sub.6 H.sub.13 763 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub .3 CH.sub.2 F 764 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CHF.sub.2 765 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 CF.sub.3 766 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 CH=CH.sub.2 767 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub .3 CH.sub.2 CH=CHCH.sub.3 768 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 CH=C(CH.sub.3).sub .2 769 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 CH=CHCl 770 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 CH=CCl.sub.2 771 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub .3 CH.sub.2 C(CH.sub.3)=CH.sub.2 772 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 C=CH 773 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 774 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 -c.propyl-2,2-Cl.s ub.2 775 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 CN 776 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 777 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 778 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 779 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 780 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 781 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 782 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 C(=O)OC.sub.2 H.sub.5 783 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub .3 C(=O)NHCH.sub.3 784 CH.sub.3 4-OC.sub.6 H.sub.4 -4-OCH.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 785 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.3 786 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl C.sub.2 H.sub.5 787 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl n-C.sub.3 H.sub.7 788 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl i-C.sub.3 H.sub.7 789 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl n-C.sub.4 H.sub.9 790 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl n-C.sub.6 H.sub.13 791 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 F 792 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CHF.sub.2 793 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 CF.sub.3 794 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 CH=CH.sub.2 795 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 CH=CHCH.sub.3 796 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 CH=C(CH.sub.3).sub.2 797 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 CH=CHCl 798 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 CH=CCl.sub.2 799 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 C(CH.sub.3)=CH.sub.2 800 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 C=CH 801 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 Si(CH.sub.3).sub.3 802 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 -c.propyl-2,2-Cl.sub.2 803 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 CN 804 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 COOC.sub.2 H.sub.5 805 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH(CH.sub.3)COOC.sub.2 H.sub.5 806 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 807 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 C.sub.6 H.sub.4 -4-F 808 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 C.sub.6 H.sub.4 -3-F 809 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl CH.sub.2 C.sub.6 H.sub.4 -2-F 810 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl C(=O)OC.sub.2 H.sub.5 811 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl C(=O)NHCH.sub.3 812 CH.sub.3 4-OC.sub.6 H.sub.4 -4-t-butyl C(=O)C(=O)OC.sub.2 H.sub.5 813 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub. 3 CH.sub.3 814 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 C.sub.2 H.sub.5 815 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 n-C.sub.3 H.sub.7 816 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 i-C.sub.3 H.sub.7 817 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 n-C.sub.4 H.sub.9 818 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 n-C.sub.6 H.sub.13 819 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 F 820 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CHF.sub.2 821 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CF.sub.3 822 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=CH.sub.2 823 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub. 3 CH.sub.2 CH=CHCH.sub.3 824 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=C(CH.sub.3).sub. 2 825 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=CHCl 826 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CH=CCl.sub.2 827 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub. 3 CH.sub.2 C(CH.sub.3)=CH.sub.2 828 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C=CH 829 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 830 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 -c.propyl-2,2-Cl.su b.2 831 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 CN 832 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 833 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 834 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 835 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 836 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 837 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 838 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 C(=O)OC.sub.2 H.sub.5 839 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub. 3 C(=O)NHCH.sub.3 840 CH.sub.3 4-OC.sub.6 H.sub.4 -4-CF.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 841 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub. 3 CH.sub.3 842 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 C.sub.2 H.sub.5 843 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 n-C.sub.3 H.sub.7 844 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 i-C.sub.3 H.sub.7 845 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 n-C.sub.4 H.sub.9 846 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 n-C.sub.6 H.sub.13 847 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 F 848 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CHF.sub.2 849 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CF.sub.3 850 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=CH.sub.2 851 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub. 3 CH.sub.2 CH=CHCH.sub.3 852 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=C(CH.sub.3).sub. 2 853 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=CHCl 854 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CH=CCl.sub.2 855 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub. 3 CH.sub.2 C(CH.sub.3)=CH.sub.2 856 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C=CH 857 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 Si(CH.sub.3).sub.3 858 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 -c.propyl-2,2-Cl.su b.2 859 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 CN 860 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 COOC.sub.2 H.sub.5 861 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH(CH.sub.3)COOC.sub.2 H.sub.5 862 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 863 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -4-F 864 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -3-F 865 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 CH.sub.2 C.sub.6 H.sub.4 -2-F 866 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 C(=O)OC.sub.2 H.sub.5 867 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub. 3 C(=O)NHCH.sub.3 868 CH.sub.3 4-OC.sub.6 H.sub.4 -2-CF.sub.3 C(=O)C(=O)OC.sub.2 H.sub.5 869 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.3 870 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl C.sub.2 H.sub.5 871 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl n-C.sub.3 H.sub.7 872 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl i-C.sub.3 H.sub.7 873 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl n-C.sub.4 H.sub.9 874 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl n-C.sub.6 H.sub.13 875 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 F 876 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CHF.sub.2 877 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 CF.sub.3 878 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CH.sub.2 879 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CHCH.sub.3 880 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=C(CH.sub.3).sub.2 881 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CHCl 882 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 CH=CCl.sub.2 883 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 C(CH.sub.3)=CH.sub.2 884 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 C=CH 885 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 Si(CH.sub.3).sub .3 886 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 -c.propyl-2,2-Cl .sub.2 887 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 CN 888 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 COOC.sub.2 H.sub.5 889 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH(CH.sub.3)COOC.sub.2 H.sub.5 890 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 891 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -4-F 892 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -3-F 893 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl CH.sub.2 C.sub.6 H.sub.4 -2-F 894 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl C(=O)OC.sub.2 H.sub.5 895 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl C(=O)NHCH.sub.3 896 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.4 -4-Cl C(=O)C(=O)OC.sub.2 H.sub.5 797 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.3 898 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 C.sub.2 H.sub.5 899 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 n-C.sub.3 H.sub.7 900 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 i-C.sub.3 H.sub.7 901 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 n-C.sub.4 H.sub.9 902 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 n-C.sub.6 H.sub.13 903 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 F 904 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CHF.sub.2 905 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CF.sub.3 906 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=CH.sub.2 907 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=CHCH.sub.3 908 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=C(CH.sub.3).sub.2 909 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=CHCl 910 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CH=CCl.sub.2 911 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C(CH.sub.3)=CH.sub.2 912 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C=CH 913 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 Si(CH.sub.3).sub.3 914 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 -c.propyl-2,2-Cl.sub .2 915 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 CN 916 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 COOC.sub.2 H.sub.5 917 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH(CH.sub.3)COOC.sub.2 H.sub.5 918 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -3-CF.sub.3 919 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -4-F 920 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -3-F 921 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 CH.sub.2 C.sub.6 H.sub.4 -2-F 922 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 C(=O)OC.sub.2 H.sub.5 923 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 C(=O)NHCH.sub.3 924 CH.sub.3 4-OCH.sub.2 C.sub.6 H.sub.3 -3,4-Cl.sub.2 C(=O)C(=O)OC.sub.2 H.sub.5______________________________________
In Tables 2.1 and 2.2, the .sup.13 C-NMR data of the compounds 1-[4-(3-trifluoromethyl-phenylmethoxy)-phenyl]-1,2-propanedione 1-E-[methyloxime]-2-oxime and 1-[4-(3-trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-Z-[methyloxime]-2-oxime (which was prepared by one of the known processes and from which the E/Z isomer mixture formed in the preparation was isolated) or, respectively, methyl 2-[[[(1-methyl-2-(4-(3-trifluoromethylphenylmethoxy)-phenyl)-2-E-[methoxyimino]ethylidene)amino]oxy]methyl]-.alpha.-(methoxymethylene)-phenylacetate (compound A225 in Table 1) are shown. The similar chemical shifts of atoms 1 and 4 of compound A in Table 2.1 and those in Table 2.2 confirm the E configuration of the compounds of the formula I.
TABLE 2.1______________________________________.sup.13 C-NMR shifts and .sup.1 J.sub.cc coupling constants of 1-[4-(3- trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-E-[methyloxime]-2-oxime (A) and 1-[4-(3- trifluoromethylphenylmethoxy)-phenyl]-1,2-propanedione 1-Z-[methyloxime]-2-oxime (B)______________________________________ #STR10## - #STR11## - Compound Atom No. Shift .delta. (ppm) Coupling .sup.1 Jcc (Hz)______________________________________ A 1 125.6 J.sub.12 = 56.0 3 155.0 J.sub.23 = 72.0 4 10.1 J.sub.34 = 43.0 B 1 127.8 J.sub.12 = 69.0 3 452.1 J.sub.23 = 56.5 4 14.4 J.sub.34 = 41.5______________________________________
TABLE 2.2______________________________________.sup.13 C-NMR shifts of methyl 2-[[[(1-methyl-2-(4-(3-trifluoromethylphenylmethoxy)- phenyl)-2-E-[methoxyimino]ethylidene)amino]oxy]methyl]- .alpha.-(methoxymethylene)-phenylacetate (compound 1.225) #STR12## - Atom No. Shift .delta. (ppm)______________________________________1 124.9 2 155.1 3 155.0 4 11.1______________________________________

Number	Name	Date
5346902	Clough et al.	Sep 1994
5371084	de Fraine et al.	Dec 1994
5387607	Brand et al.	Feb 1995
5563168	Brand et al.	Oct 1996

Number	Date	Country
9178167	Dec 1991	AUX
9526710	May 1996	AUX
0370629	May 1990	EPX
0414153	Feb 1991	EPX
0460575	Dec 1991	EPX
0463488	Jan 1992	EPX
0472300	Feb 1992	EPX
0506149	Sep 1992	EPX
0617014	Sep 1994	EPX
9007493	Jul 1990	WOX
9213830	Aug 1992	WOX
9218494	Oct 1992	WOX
9218487	Oct 1992	WOX
9518789	Jul 1995	WOX
9521156	Aug 1995	WOX
9521154	Aug 1995	WOX
9521153	Aug 1995	WOX
9534526	Dec 1995	WOX
9611183	Apr 1996	WOX
9616026	May 1996	WOX
9632373	Oct 1996	WOX
9635669	Nov 1996	WOX

Process for the preparation of pesticides

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Derwent Abstract 97-011705 (1997).
Derwent Abstract 95-292864 (1995).
Derwent Abstract 95-292863 (1995).
Derwent Abstract 95-292862 (1995).
Derwent Abstract 96-477039 (1996).