Herbicidal cyclohexane-1,3-dione derivatives

This invention relates to organic compounds having biological activity and in particular to organic compounds having herbicidal properties and plant growth regulating properties, to processes for the preparation of such compounds, to intermediates useful in the preparation of such compounds and to herbicidal compositions and processes utilizing such compounds and processes utilizing such compounds.
The use of certain cyclohexane-1,3-dione derivatives as grass herbicides is known in the art. For example, the "Pesticide Manual" (C. R. Worthing Editor, The British Crop Protection Council, 6th Edition 1979) describes the cyclohexane-1,3-dione derivative known commercially as alloxydim-sodium (methyl 3-[1-(allyloxyimino)butyl]-4-hydroxy-6,6-dimethyl-2-oxocyclohex-3-ene carboxylate) and its use as a grass herbicide. This compound is disclosed in Australian Pat. No. 464 655 and its equivalents such as UK Pat. No. 1 461 170 and U.S. Pat. No. 3,950,420.
A variety of herbicidal compounds containing substituted phenyl cyclohexane-1,3-diones are described in the art. For example, French Pat. No. 2,518,990, as well as the published British Patent application equivalent thereto, viz., No. 2,116,544 describe various 5-(4-substituted phenyl) cyclohexane-1,3-diones and European Patent Application No. 085,529 describes various 5-(polysubstituted phenyl) cyclohexane-1,3-diones and their herbicidal properties.
It has now been found that a new group of cyclohexane-1,3-dione derivatives which have a 5-mesityl substituent which is in turn substituted with a carboxymethyl derivative, exhibit exceptionally high general grass-killing activity.
Accordingly the invention provides a compound of formula I ##STR2## wherein X is cyano or ##STR3## in which R.sup.5 and R.sup.6 are each independently hydrogen or C.sub.l to C.sub.6 alkyl and
Y is oxygen or sulfur;
Z is selected from the group consisting of hydrogen, halogen, C.sub.1 to C.sub.4 alkyl, C.sub.1 to C.sub.4 alkanoyl, sulfamoyl, C.sub.1 to C.sub.4 alkylsulfamoyl, di(C.sub.1 to C.sub.4 alkyl)sulfamoyl, carboxy and trifluoroacetylamino;
R.sup.1 is selected from the group consisting of: hydrogen; an acyl group; and an inorganic or organic cation;
R.sup.2 is selected from the group consisting of: C.sub.1 to C.sub.6 alkyl; C.sub.2 to C.sub.6 alkenyl; C.sub.2 to C.sub.6 haloalkenyl; C.sub.2 to C.sub.6 alkynyl; and substituted C.sub.1 to C.sub.6 alkyl wherein the alkyl group is substituted with a substituent selected from the group consisting of halogen, phenyl, and substituted phenyl wherein the benzene ring is substituted with from one to three substituents selected from the group consisting of halogen, and C.sub.1 to C.sub.6 alkyl;
R.sup.3 is selected from the group consisting of: C.sub.1 to C.sub.6 alkyl; and
R.sup.4 is selected from the group consisting of: hydrogen; C.sub.1 to C.sub.6 alkyl; and (C.sub.1 to C.sub.6 alkoxy) carbonyl.
When in the compound of formula I R.sup.1 is chosen from acyl the nature of the acyl group is not narrowly critical. Although not intending to be bound by theory, it is believed that when R.sup.1 is acyl the acyl group may be removed in the plant by hydrolysis to give the corresponding compound of formula I in which R.sup.1 is hydrogen. Suitable acyl groups include: alkanoyl, for example C.sub.2 to C.sub.6 alkanoyl; aroyl, for example benzoyl and substituted benzoyl wherein the benzene ring is substituted with from one to three substituents chosen from the group consisting of halogen, nitro, cyano, C.sub.1 to C.sub.6 alkyl, C.sub.1 to C.sub.6 haloalkyl, C.sub.1 to C.sub.6 alkoxy and C.sub.1 to C.sub.6 alkylthio.
When in the compound of formula I R.sup.1 is chosen from an inorganic or organic cation the nature of the cation is not narrowly critical. Although not intending to be bound by theory, it is believed that when R.sup.1 is a cation the cation may be removed in the plant to give a compound of formula I wherein R.sup.1 is hydrogen. Suitable inorganic cations include the alkali and alkaline earth metal ions, heavy metal ions including the transition metal ions, and the ammonium ion. Suitable organic cations include the cation R.sup.7 R.sup.8 R.sup.9 R.sup.10 N.sup..sym. wherein R.sup.7, R.sup.8, R.sup.9 and R.sup.10 are independently chosen from the group consisting of: hydrogen; C.sub.1 to C.sub.10 alkyl; substituted C.sub.1 to C.sub.10 alkyl wherein the alkyl group is substituted with a substituent chosen from the group consisting of hydroxy, halogen and C.sub.1 to C.sub.6 alkoxy; phenyl; benzyl; and the groups substituted phenyl and substituted benzyl wherein the benzene ring is substituted with from one to three substituents chosen from the group consisting of halogen, nitro, cyano, C.sub.1 to C.sub.6 alkyl, C.sub.1 to C.sub.6 haloalkyl, C.sub.1 to C.sub.6 alkoxy and C.sub.1 to C.sub.6 alkylthio.
The compounds of the invention may exist in two isomeric forms as shown below, wherein .phi. represents the group ##STR4##
It should be recognized that when R.sub.1 is hydrogen the compounds of the invention may exist in any one of four tautomeric forms as shown below wherein .phi. represents the group ##STR5##
Preferred compounds of the invention include those compounds of formula I wherein:
the substituent X is chosen from cyano, carbamoyl and thiocarbamoyl;
Z is selected from hydrogen, methyl, C.sub.1 to C.sub.4 alkanoyl, sulfamoyl, dimethylsulfamoyl and trifluoroacetylamino;
R.sup.1 is selected from hydrogen, the alkalai metal cations, C.sub.2 to C.sub.6 alkanoyl, benzoyl and substituted benzoyl wherein the benzoyl ring is substituted with from one to three substituents chosen from halogen, nitro and cyano.
R.sup.2 is selected form the group consisting of C.sub.1 to C.sub.4 alkyl, C.sub.2 to C.sub.4 alkeynyl, C.sub.3 to C.sub.4 alkynyl, C.sub.1 to C.sub.4 haloalkyl and C.sub.2 to C.sub.4 halo alkeynyl;
R.sup.3 is selected from C.sub.1 to C.sub.6 alkyl; and
R.sup.4 is hydrogen.
More preferred compounds of the invention include those compounds of formula I wherein:
X is cyano or thiocarbamoyl;
Z is selected from hydrogen, methyl or acetyl;
R.sup.1 is selected from hydrogen and the alkali metal cations;
R.sup.2 is selected from methyl, ethyl, n-propyl, allyl, propargyl and 3-chloroallyl;
R.sup.3 is selected from methyl, ethyl and n-propyl;
R.sup.4 is hydrogen.
Examples of compounds embraced by the invention include: ##STR6##
Specific examples of the compounds of the invention include those compounds detailed in Table 1 below.
TABLE 1______________________________________ ##STR7##CompoundNo X Z______________________________________1 CN COCH.sub.32 CONH.sub.2 COCH.sub.33 CSNH.sub.2 COCH.sub.34 CN H5 CONH.sub.2 H6 CSNH.sub.2 H7 CON(CH.sub.3).sub.2 H______________________________________
The compounds of the invention may be prepared by a variety of methods and in a further aspect the invention provides methods for the preparation of compounds of formula I.
Conveniently the preparation of the invention can be considered in four or five parts.
Part A involves the formation of a 5-arylcyclohexan-1,3-dione of formula IX. This reaction may be carried out in a two step process by:
(i) reacting, preferably in the presence of a base, an aldehyde derivative of formula V with acetone (IVa) or an acetone derivative of formula IVb to form a ketone derivative of formula VIa or VIb respectively; and reacting, preferably in the presence of a base, a ketone derivative of formula VIa with a malonic acid ester derivative of formula VIIa or a ketone derivative of formula VIb with a malonic acid ester of formula VIIb, to give an intermediate of formula VIIIa or VIIIb respectively which may be isolated or hydrolysed directly, preferably in the presence of an acid, to give a 5-arylcyclohexan-1,3-dione of formula IX.
(ii) reacting, preferably in the presence of a base, an aldehyde derivative of formula V with an acetic acid ester of formula IVc to give a 2-arylalkenoate derivative of formula VIc which is in turn reacted, preferably in the presence of a base, with an acetoacetic acid ester derivative of formula VIIc to give an intermediate of formula VIIIa which may be isolated or hydrolysed directly, preferably in the presence of an acid, to give a 5-arylcyclohexan-1,3-dione of formula IX.
Part B involves the acylation of a compound of formula IX to give a 2-acylcyclohexane-1,3-dione derivative of formula Xa. Alternatively Part B involves the acylation of a compound of formula VIIIa or VIIIb to give a 2-acylcyclohexane-1,3-dione derivative of formula XIa or XIb respectively which may be hydrolysed, preferably in the presence of a base, to give a 2-acylcyclohexane-1,3-dione of formula Xa. The acylation reaction may be carried out by reacting a cyclohexane-1,3-dione derivative of formula VIII or IX with:
(i) an acid anhydride of formula XII in the presence of either an alkali metal salt of the corresponding acid of formula XV or an alkoxide salt of formula XIV, wherein M is an alkali metal ion and R is C.sub.1 to C.sub.6 alkyl; or
(ii) an acid anhydride of formula XII in the presence of the corresponding acid of formula XV, preferably in the presence of a Lewis acid or strong proton acid catalyst; or
(iii) with an alkali or alkaline earth metal hydride followed by reaction with an acid anhydride of formula XII or an acid halide of formula XVI; or
(iv) an acid anhydride of formula XII in the presence of a strong organic base such as 4-dimethylaminopyridine or imidazole.
Alternatively, this acylation reaction may be carried out by:
(v) reacting a cyclohexane-1,3-dione derivative of formula VIII or formula IX with an acid halide of formula XVI in the presence of a base to give an intermediate O-acyl derivative of the type of formula XVII; and
(vi) reacting the intermediate of formula XVII with a Lewis acid or strong proton acid catalyst; or
(vii) reacting the intermediate of formula XVII with a suitable strong organic base such as 4-dimethylaminopyridine.
Part C involves the reaction of a compound of formula Xa by electrophilic aromatic chloromethylation to give a compound of formula Xb which may readily be converted to a compound of formula Xc (X =CN). Alternatively compound Xc may be formed by electrophilic aromatic substitution of compound Xd.
Part D involves the formation of a compound of the invention of formula I wherein R.sup.1 is hydrogen, that is a compound of formula II. This reaction may be carried out either by reacting a 2-acyl cyclohexane-1,3-dione of formula Xc with:
(i) an alkoxyamine derivative of formula XVIII, or
(ii) hydroxylamine to give an intermediate oxime derivative of formula XIX and reacting that intermediate oxime derivative of formula XIX with an alkylating agent of formula XX, wherein L is a leaving group such as, for example, chloride, bromide, iodide, sulfate, nitrate, methyl sulfate, ethyl sulfate, tetrafluoroborate, hexafluorophosphate, hexafluoroantimonate, methanesulfonate, fluorosulfonate, fluoromethanesulfonate and trifluoromethanesulfonate.
Part E involves the formation of a compound of the invention of formula I wherein R.sup.1 is a substituent other than hydrogen.
Compounds of the invention of formula I, wherein R.sup.1 forms an acyl derivative of a compound of formula II, may be prepared from the corresponding compounds of the invention of formula II by reacting with an acylation reagent of formula XXI, wherein L is a leaving group preferably a halogen.
Compounds of the invention of formula I wherein R.sup.1 is an inorganic or organic cation may be prepared from the compounds of the invention of formula I wherein R.sup.1 is hydrogen, that is, compounds of formula II, by reacting said compounds of formula II with an inorganic or organic salt. For example, the compounds of formula I wherein R.sup.1 is an alkali metal ion may be prepared by reacting the appropriate compound of formula II with the appropriate alkali metal hydroxide or alkoxylate. The compounds of formula I wherein R.sup.1 is a transition metal ion or an organic cation may similarly be prepared by reacting the appropriate compound of formula II with an appropriate transition metal salt or organic base. Alternatively, the compounds of formula I wherein R.sup.1 is a transition metal ion or an organic cation may be prepared by reacting the appropriate compound of formula I wherein R.sup.1 is an alkali metal ion with an appropriate transition metal salt or organic salt.
Accordingly, in a further aspect the invention provides a process for the preparation of a compound of formula I, as hereinbefore defined, which process comprises:
reacting a 2-acylcyclohexane-1,3-dione derivative of formula Xc with an alkoxyamine derivative of formula XVIII to give a compound of the invention of formula II or reacting the 2-acylcyclohexane-1,3-dione derivative of formula Xc with hydroxylamine and alkylating the oxime intermediate of formula XIX with an alkylating agent of formula XX, wherein L is a leaving group, to give a compound of the invention of formula II; and optionally
reacting the compound of the invention of formula II with a compound of formula XXI wherein L is a leaving group, to give a compound of the invention of formula I.
Certain of the intermediate compounds of formula Xc, are novel compounds and therefore in further embodiments the invention provides novel compounds of formula Xc, and processes for the preparation thereof.
The structures of the compounds described above are detailed in the following. ##STR8##
The compounds of formula I are active as herbicides and therefore, in a further aspect the invention provides a process for severely damaging of killing unwanted plants which process comprises applying to the plants, or to the growth medium of the plants, an effective amount of a compound of formula I as hereinbefore defined.
Generally speaking the comounds of the formula I are herbicidally effective against monocotyledonous plants, dicotyledonous plants being relatively unaffected by rates of application of the compounds of the invention which are severely damaging or lethal to most grass species.
Accordingly, in yet a further aspect the invention provides a process for controlling monocotyledonous weeds in cultivated crops, which process comprises applying to the crop, or to the growth medium of the crop, a compound of formula I, as hereinbefore defined, in an amount sufficient to severely damage or kill the weeds but insufficient to damage the crop substantially.
The compounds of formula I may be applied directly to the plant (post-emergence application) or to the soil before the emergence of the plant (pre-emergence application). However, the compounds are, in general, more effective when applied to the plant post-emergence.
The compounds of formula I may be used on their own to inhibit the growth of, severly damage, or kill plants but are preferably used in the form of a composition comprising a compound of the invention in admixture with a carrier comprising a solid or liquid diluent. Therefore, in yet a further aspect the invention provides growth inhibiting, plant damaging, or plant killing compositions comprising a compound of formula I as hereinbefore defined and an inert carrier therefor.
Certain of the compounds of formula I exhibit useful plant growth regulating activity. For example, while compounds of formula I are selectivity active herbicides against wild grasses in crops of cultivated plants at some rates of application they exhibit plant growth regulating effects in said crops.
Plant growth regulating effects may be manifested in a number of ways. For example, raising the sugar content of plants, suppression of apical dominance, stimulation of auxiliary bud growth, stimulation of early flowering and seed formation, enhancement of flowering and increase in seed yield, stem thickening, stem shortening and tillering. Plant growth regulating effects shown in compounds of the invention may include, for example, tillering and stem shortening in crops such as wheat and barley, and increasing the sugar content of sugar cane.
Accordingly in a still further aspect the invention provides a process for regulating the growth of a plant which process comprises applying to the plant, to the seed of the plant, or to the growth medium of the plant, an effective amount of a compound of formula I, as hereinbefore defined.
To effect the plant growth regulating process of the present invention the compounds of formula I may be applied directly to the plant (post-emergence application) or to the seed or soil before the emergence of the plant (pre-emergence) application.
The compounds of formula I may be used on their own to regulate the growth of plants but in general are preferably used in the form of a composition comprising a compound of the invention in admixture with a carrier comprising a solid or liquid diluent. Therefore, in a still further aspect the invention provides plant growth regulating compositions comprising a compound of formula I as hereinbefore defined and an inert carrier therefor.
The compositions of the present invention may be in the form of solids, liquids or pastes. The compositions include both dilute compositions which are ready for immediate use and concentrated compositions which may require dilution before use. Therefore, the concentration of the active ingredient in the compositions of the present invention will vary depending on the types of formulation and whether the composition is ready for use such as, for example, a dust formulation or an aqueous emulsion or whether the composition is a concentrate such as, for example, an emulsifiable concentrate or a wettable powder, which is suitable for dilution before use. In general the compositions of the present invention comprise from 1 ppm to 99% by weight of active ingredient.
The solid compositions may be in the form of powders, dusts, pellets, grains, and granules wherein the active ingredient is mixed with a solid diluent. Powders and dusts may be prepared by mixing or grinding the active ingredient with a solid carrier to give a finely divided composition. Granules, grains and pellets may be prepared by bonding the active ingredient to a solid carrier, for example, by coating or impregnating the preformed granular solid carrier with the active ingredient or by agglomeration techniques.
Examples of solid carriers include: mineral earths and clays such as, for example, kaolin, bentonite, kieselguhr, Fuller's earth, Attaclay, diatomaceous earth, bole, loess, talc, chalk, dolomite, limestone, lime, calcium carbonate, gypsum, calcium sulfate, pyrophyllite, silicic acid, silicates and silica gels; fertilizers such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate and urea; natural products of vegetable origin such as, for example, grain meals and flours, bark meals, wood meals, nutshell meals and cellulosic powders; and synthetic polymeric materials such as, for example, ground or powdered plastics and resins.
Alternatively, the solid compositions may be in the form of dispersible or wettable dusts, powders, granules or grains wherein the active ingredient and the solid carrier are combined with one or more surface active agents which act as wetting, emulsifying and/or dispersing agents to facilitate the dispersion of the active ingredient in liquid.
Examples of surface active agents include those of the cationic, anionic and non-ionic type. Cationic surface active agents include quaternary ammonium compounds, for example, the long chain alkylammonium salts such as cetyltrimethylammonium bromide. Anionic surface active agents include: soaps or the alkali metal, alkaline earth metal and ammonium salts of fatty acids; the alkali metal, alkaline earth metal and ammonium salts of ligninsulfonic acid; the alkali metal, alkaline earth metal and ammonium salts of arylsulfonic acids including the salts of naphthalenesulfonic acids such as butylnaphthalenesulfonic acids, the di- and tri- isopropylnaphthalenesulfonic acids, the salts of the condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, the salts of the condensation products of sulfonated naphthalene and naphthalene derivatives with phenol and formaldehyde, and the salts of alkylarylbenzenesulfonic acids such as dodecylbenzenesulfonic acid; the alkali metal, alkaline earth metal and ammonium salts of the long chain mono esters of sulfuric acid or alkylsulfates such as laurylsulfate and the mono esters of sulfuric acid with fatty alcohol glycol ethers. Nonionic surface active agents include: the condensation products of ethylene oxide with phenols and alkylphenols such as isooctylphenol, octylphenol and nonylphenol; the condensation products of ethylene oxide with castor oil; the partial esters derived from long chain fatty acids and hexitol anhydrides, for example sorbitan monolaurate, and their condensation products with ethylene oxide; ethylene oxide/propylene oxide block copolymers; lauryl alcohol polyglycol ether acetal; and the lecithins.
The liquid compositions may comprise a solution or dispersions of the active ingredient in a liquid carrier optionally containing one or more surface active agents which act as wetting, emulsifying and/or dispersing agents. Examples of liquid carriers include: water; mineral oil fractions such as, for example, kerosene, solvent naphtha, petroleum, coal tar oils and aromatic petroleum fractions; aliphatic, cycloaliphatic and aromatic hydrocarbons such as, for example, paraffin, cyclohexane, toluene, the xylenes, tetrahydronaphthalene and alkylated naphthalenes; alcohols such as, for example, methanol, ethanol, propanol, isopropanol, butanol, cyclohexanol and propylene glycol; ketones such as, for example, cyclohexanone and isophorone; and strongly polar organic solvents such as, for example, dimethylformamide, dimethylsulfoxide, N-methylpyrrolidone and sulfolane.
A preferred liquid composition comprises an aqueous suspension, dispersion or emulsion of the active ingredient which is suitable for application by spraying, atomizing or watering. Such aqueous compostions are generally prepared by mixing concentrated compositions with water. Suitable concentrated compositions include emulsion concentrates, pastes, oil dispersions, aqueous suspensions and wettable powders. The concentrates are usually required to withstand storage for prolonged periods and after such storage to be capable of dilution with water to form aqueous preparations which remain homogeneous for a sufficient time to enable them to be applied by conventional spray equipment. The concentrates conveniently contain from 10 to 99%, preferably 10 to 60%, by weight of active ingredient.
Emulsion or emulsifiable concentrates are conveniently prepared by dissolving the active ingredient in an organic solvent containing one or more surface active agents and optionally an oil. Oil dispersions may be prepared by grinding together the active ingredient, a hydrocarbon oil, and one or more surface active agents. Aqueous suspension concentrates may conveniently be prepared by ball milling a mixture of the active agent and preferably at least one suspending agent. Suitable suspending agents include: hydrophilic colloids such as, for example, poly(N-vinylpyrrolidone), sodium carboxymethylcellulose and the vegetable gums, gum acacia and gum tragacanth; hydrated colloidal mineral silicates such as, for example, montmorillonite, beidellite, nontronite, hectorite, saponite, sauconite and bentonite; other cellulose derivatives; and poly(vinyl alcohol). Wettable powder concentrates may conveniently be prepared by blending together the active ingredient, one or more surface active agents, one or more solid carriers and optionally one or more suspending agents and grinding the mixture to give a powder having the required particle size.
The aqueous suspensions, dispersions or emulsions may be prepared from the concentrated compositions by mixing the concentrated compositions with water optionally containing surface active agents and/or oils.
It should be noted that the compounds of the invention of formula I wherein R.sup.1 is hydrogen are acidic. Therefore, the compounds of formula I may be formulated and applied as the salts of organic or inorganic bases. In formulating and employing the compounds of formula I in the form of their salts either the salts per se, that is the compounds of formula I wherein R.sup.1 is an inorganic or an organic cation, may be used in the formulation or the compounds of formula I wherein R.sup.1 is hydrogen may be used in the formulation and the salts generated in situ by the use of the appropriate organic or inorganic base.
The mode of application of the compositions of the invention will depend to a large extent on the type of composition used and the facilities available for its application. Solid compositions may be applied by dusting or any other suitable means for broadcasting or spreading the solid. Liquid compositions may be applied by spraying, atomizing, watering, introduction into the irrigation water, or any other suitable means for broadcasting or spreading the liquid.
The rate of application of the compounds of the invention will depend on a number of factors including, for example, the compound chosen for use, the identity of the plants whose growth is to be inhibited the formulations selected for use and whether the compound is to be applied for foliage or root uptake. As a general guide, however, an application rate of from 0.005 to 20 kilograms per hectate is suitable while from 0.01 to 5.0 kilograms per hectare may be preferred.
The compositions of the invention may comprise, in addition to one or more compounds of the invention, one or more compounds not of the invention but which possess biological activity. For example, as hereinbefore indicated the compounds of the invention are in general substantially more effective against monocotyledonous plants or grass species than against dicotyledonous plants or broad-leaved species. As a result, in certain applications the herbicidal use of the compounds of the invention alone may not be sufficient to protect a crop. Accordingly in yet a still further embodiment the invention provides a herbicidal composition comprising a mixture of at least one herbicidal compound of formula I as hereinbefore defined with at least one other herbicide.
The other herbicide may be any herbicide not having the formula I. It will generally be a herbicide having a complementary action. For example, one preferred class is of mixtures comprising a herbicide active against broad-leaved weeds. A second preferred class is of mixtures comprising a contact herbicide. Examples of useful complementary herbicides include:
A. benzo-2,1,3,-thiadiazin-4-one-2,2-dioxides such as 3-isopropylbenzo-2,1,3-thiadiazin-4-one-2,2-dioxide (common name bentazon);
B. hormone herbicides and in particular the phenoxyalkanoic acids such as 4-chloro-2-methylphenoxy acetic acid (common name MCPA), 2-(2,4-dichlorophenoxy)propionic acid (common name dichlorprop), 2,4-dichlorophenoxy acetic acid (common name 2,4,-D) 2,4,5-trichlorophenoxyacetic acid (common name 2,4,5-T), 4-(4-chloro-2-methylphenoxy)butyric acid (common name MCPB), 4-(2,4-dichlorophenoxy)butyric acid (common name 2,4-DB), 2-(4-chloro-2-methylphenoxy)propionic acid (common name mecoprop), and their derivatives (eg salts, esters, amides and the like);
C. 3-[4-(4-halophenoxy)phenyl]-1,1-dialkylureas such as 3-[4-(4-chlorophenoxy)phenyl]-1,1-dimethylurea (common name chloroxuron);
D. dinitrophenols and their derivatives (eg acetates) such as 2-methyl-4,6-dinitrophenol (common name DNOC), 2-tertiarybutyl-4,6-dintrophenol (common name dinoterb), 2-secondarybutyl-4,6-dinitrophenol (common name dinoseb) and its ester dinoseb acetate;
E. dinitroaniline herbicides such as N',N'-diethyl-2,6-dinitro-4-trifluoromethyl-m-phenylenediamine acetate; (common name dinitramine), 2,6-dinitro-N,N-dipropyl-4-trifluoromethylaniline (common name trifluralin) and 4-methylsulfonyl-2,6-dinitro-N,N-dipropylaniline (common name nitralin);
F. phenylurea herbicides such as N'-(3,4-dichlorophenyl)-N,N-dimethylurea (common name diuron) and N,N-dimethyl-N'-[3-(trifluoromethyl)phenyl]urea (common name fluometuron);
G. phenylcarbamoyloxyphenylcarbamates such as 3-[(methoxycarbonyl)amino]phenyl (3-methylphenyl)carbamate (common name phenmedipham) and 3-[(ethoxycarbonylamino]phenyl phenylcarbamate (common name desmedipham);
H. 2-phenylpyridazin-3-ones such as 5-amino-4-chloro-2-phenylpyridazin-3-one (common name pyrazon);
I. uracil herbicides such as 3-cyclohexyl-5,6-trimethyleneuracil (common name lenacil), 5-bromo-3-sec-butyl-6-methyluracil (common name bromacil) and 3-tert-butyl-5-chloro-6-methyluracil (common name terbacil);
J. triazine herbicides such as 2-chloro-4-ethylamino-6-(iso-propylamino)-1,3,5-triazine (common name atrazine). 2-chloro-4,6-di(ethylamino)-1,3,5triazine (common name simazine) and 2-azido-4-(iso-propylamino)-6-methylthio-1,3,5-triazine (common name aziproptryne);
K. 1-alkoxy-2-alkyl-3-phenylurea herbicides such as 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea (common name linuron), 3-(4-chlorophenyl)-1-methoxy-1-methylurea (common name monolinuron) and 3-(4-bromo-4-chlorophenyl)-1-methoxy-1-methylurea (common name chlorobromuron);
L. Pyridine herbicides such as 3,6-dichloropicolinic acid (common name clopyralid) and 4-amino-3,5,6-trichloropicolinic acid (common name picloram);
M. 1,2,4-triazin-5-one herbicides such as 4-amino-4,5-dihydro-3-methyl-6-phenyl-1,2,4-triazine-5-one (common name metamitron) and 4-amino-6-tert-butyl 4,5-dihydro-3-methylthio-1,3,4-triazin-5-one (common name metribuzin);
N. benzoic acid herbicides such as 2,3,6-trichlorobenzoic acid (common name 2,3,6-TBA), 3,6-dichloro-2-methoxybenzoic acid (common name dicamba) and 3-amino-2,5-dichlorobenzoic acid (common name chloramben);
O. anilide herbicides such as N-butoxymethyl-.alpha.-chloro-2',6'-diethylacetanilide (common name butachlor), the corresponding N-methoxy compound (common name alachlor), the corresponding N-isopropyl compound (common name propachlor) and 3',4'-dichloropropionanilide (common name propanil);
P. dihalobenzonitrile herbicides such as 2,6-dichlorobenzonitrile (common name dichlobenil), 3,5-dibromo-4-hydroxybenzonitrile (common name bromoxynil) and 3,5-diiodo-4-hydroxybenzonitrile (common name ioxynil);
Q. haloalkanoic herbicides such as 2,2-dichloropropionic acid (common name dalapon), trichloroacetic acid (common name TCA) and salts thereof;
R. diphenylether herbicides such as 4-nitrophenyl 2-nitro-4-trifluoromethylphenyl ether (common name fluorodifen), methyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoate (common name bifenox), 2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acid and 2-chloro-4-trifluoromethylphenyl 3-ethoxy-4-nitrophenyl ether;
S. N-(heteroarylaminocarbonyl)benzenesulfonamides such as 2-chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesulfonamide (commonly known as DPX 4189);
T. Aryloxyphenoxypropionate herbicides such as butyl 2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionate (common name fluazifop) and methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propionate (common name diclofop); and
U. miscellaneous herbicides including N,N-dimethyldiphenylacetamide (common name diphenamid), N-(1-naphthyl)phthalamic acid (common name naptalam) and 3-amino-1,2,4-triazole.
Examples of useful contact herbicides include:
V. bipyridylium herbicides such as those in which the active entity is the 1,1'-dimethyl-4,4'-dipyridylium ion (common name paraquat) and those in which the active entity is the 1,1'-ethylene-2,2'-dipyridylium ion (common name diquat);
W. organoarsenical herbicides such as monosodium methanearsonate (common name MSMA); and
X. amino acid herbicides such as N-(phosphonomethyl)glycine (common name glyphosate) and its salts and esters.
The invention is now illustrated by, but in no way limited to, the following Examples.

EXAMPLE 1
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[3-acetyl-5-cyanomethyl-2,4,6-trimethylphenyl]cyclohex-2-en-1-one (1)
(i) A solution of 3-hydroxy-5-mesityl-2-propionylcyclohex-2-en-1-one (10 g, 35 mmol) in methylenechloride (50 ml) was added to a suspension of aluminium chloride (9.32 g, 70 mmol). Stirring was continued for 10 min. To the stirred ice cooled mixture was added dropwise chloromethyl methyl ether (4.19 g, 52 mmol) followed by stannic chloride (2.87 g, 11 mmol). The mixture was allowed to stir at room temperature for 1 h when 10% hydrochloric acid solution (50 ml) was added. The two phases were stirred at 50.degree. for 30 min, then separated. The organic layer was washed with water until the washings were neutral, dried over anhydrous sodium sulfate and concentrated to yield a clear yellow oil (10.6 g, 91%). Purification by chromatography over silica gel (elution with methylenechloride gave 2-propionyl-5-(3-chloromethyl-2,4,6-trimethyl phenyl)-3-hydroxy cyclohex-2-en-1-one as a clear oil (9.3 g, 80%). Proton magnetic resonance spectrum (CDCl.sub.3 ; .delta. in ppm): 1.15 (3H,t,J7 Hz); 2.32 (6H,s); 2.47 (3H,s); 2.5-4.1 (7H,brm); 4.62(2H,s); 6.85 (1H,s); 18.20 (1H,s).
(ii) A solution of 3-hydroxy 2-propionyl-5-(3-chloromethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (3.32, 9.96 mmol) in dmf (15 ml) was added to a suspension of sodium cyanide (0.98, 19.9 mmol) in dmf (10 ml). The mixture was stirred at 70.degree. for 4 h, then cooled and partitioned between methylene choride and water. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Chromatography on silica gel (elution with an increasing gradient of ethyl acetate in methylene chloride) gave 3-hydroxy-2-propionyl-5-(3-cyanomethyl-2,4,6-trimethylphenyl) cyclohex-2-en-1-one (2.65 g, 81%) plus a further impure fraction. Proton magnetic resonance spectrum (CDCl.sub.3, .delta. in ppm): 1.18 (3H,t,J7 Hz); 2.33 (3H,s); 2.37 (3H,s); 2.42 (3H,s); 2.5-4.1(7H,m); 3.62 (2H,s); 7.90 (1H,s); 18.20 (1H,s). Infrared spectrum: .nu. (CHCl.sub.3) 2250 m cm.sup.-1.
(iii) Acetyl chloride (1.34 g, 17.0 mmol) was added to an ice cooled mixture of 3-hydroxy-2-propionyl-5-(3-cyanomethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (2.65 g, 8.15 mmol) and aluminium chloride (4.15 g, 33.4 mmol) in carbon disulfide (100 ml). The mixture was refluxed for 4 h, cooled and added cautiously to 10% hydrochloric acid (50 ml) and ice (50 ml). The organic solvent was allowed to evaporate from the mixture then the aqueous layer was extracted with ethyl acetate, the organic extracts were washed with water, dried over sodium sulfate and concentrated under reduced pressure. The crude product was chromatographed on silica gel (elution with an increasing gradient of ethyl acetate in methylene chloride). After an initial fraction of unreacted starting material, 3-hydroxy-2-propionyl-5-(3-acetyl-5-cyanomethyl-2,4,6-trimethyl phenyl)cyclohex-2-en-1-one was obtained as a colourless solid (1.5 g, 50%), which was characterized by proton magnetic resonance spectroscopy (CDCl.sub.3 ; .delta. in ppm): 1.12 (3H,t); 2.23 (3H,s); 2.25 (3H,s); 2.47 (6H,s); 2.4-4.1 (7H,m); 18.08 (1H,s).
(iv) Ethoxyaminehydrochloride (0.17 g, 1.76 mmol) and sodium acetate (0.14 g, 1.76 mmol) were added to a solution of the cyanomethyl compound prepared in part (iii) above (0.43 g, 1.17 mmol) in ethanol (20 ml). Stirring was continued for 18 h at 20.degree.. The solvent was removed under reduced pressure and the residue was partitioned between water and methylene chloride. The organic layer was washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure to give 2-[1-(ethoxyimino)propyl]-3-hydroxy-5-(3-acetyl-5-cyanomethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (1) as a yellow oil (0.48 g, 100%). The compound was characterized by proton magentic resonance spectroscopy and the spectroscopic data are reported in Table 2.
EXAMPLE 2
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-acetyl-5-carbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (2)
(i) A solution of 2-propionyl-3-hydroxy-5-(3-acetyl-5-cyanomethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (0.67 g, 1.83 mmol) in 5% aqueous sodium hydroxide (12 ml) was refluxed for 30 min. The solution was then cooled, acidified and extracted with ethylacetate. The organic layer was washed with water, saturated aqueous sodium hydrogen carbon solution, further water then dried over anhydrous sodium sulfate. The solvent was then evaporated under reduced pressure to yield 2-propionyl-3-hydroxy-5-(3-acetyl-5-carbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one as a colourless solid (0.49 g, 65%). The compound was characterized by proton magnetic resonance spectroscopy (CDCl.sub.3 ; .delta. in ppm): 1.14 (3H,t); 2.13 (3H,s); 2.22 (3H,s); 2.32 (3H,s); 2.46 (3H,s); 2.4-3.9 (7H, m); 3.61 (2H,s); 5.48 (1H,brs); 6.10 (1H,brs); 18.00 (1H,brs). The sodium hydrogen carbonate solution washings were acidified and extracted with ethylacetate. The organic layer was washed with water, dried over sodium sulfate and concentrated under reduced pressure to yield 2-[3-(4-propionyl-5-hydroxycyclohex-3-one-4- enyl)-5-acetyl-2,4,6-trimethylphenyl]acetic acid (0.11 g, 16%) as a colourless solid.
(ii) 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-acetyl-5-carbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (2) was prepared from the above precursor as described in Example 1 part (iv). The compound was characterized by proton magnetic resonance spectroscopy. The spectroscopic data are reported in Table 2.
EXAMPLE 3
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-acetyl-5-thiocarbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (3)
(i) A solution of 2-propionyl-3-hydroxy-5-(3-acetyl-5-cyanomethyl-2,4,6-trimethylphenyl-cyclohex-2-en-1-one (0.40 g, 1.0 mmol) and thioacetamide (0.16 g, 2.2 mmol) in dmf (10 ml) was saturated with anhydrous hydrogen chloride. The solution was then heated under a distillation head for 45 min at 110.degree.. Most of the dmf was then removed by distillation under reduced pressure and water was added. The aqueous solution was neutralized and extracted with ethylacetate. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated. The crude product was recrystallized from ethanol to yield 2-propionyl-3-hydroxy-5-(3-acetyl-5-thiocarbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one as colourless crystals (0.26 g, 65%). The compound was characterized by proton magnetic resonance spectroscopy (CDCl.sub.3 ; .delta. in ppm): 1.14 (3H,t); 2.12 (3H,s); 2.23 (3H,s); 2.30 (3H,s); 2.44 (3H,s); 3.05 (2H,q); 2.4- 4.2 (5H,m); 4.12 (2H,s); 6.50 (1H,brs); 7.45 (1H,brs); 18.05 (1H,s).
(ii) 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-acetyl-5-thiocarbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (3) was prepared from the above thioamide as described in Example 1 part (iv). The compound was characterized by proton magnetic resonance spectroscopy. The spectroscopic data are reported in Table 2.
EXAMPLE 4
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[3-cyanomethyl-2,4,6-trimethylphenyl]cyclohex-2-en-1-one (4)
(i) 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[3-cyanomethyl-2,4,6-trimethylphenyl]cyclohex-2-en-1-one was prepared as described in Example 1 part (iv) from the corresponding nitrile prepared in Example 1 part (ii). The compound was characterized by proton magnetic resonance spectroscopy and the spectroscopic data are recorded in Table 2.
EXAMPLE 5
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[3-carbamoylmethyl-2,4,6-trimethylphenyl]cyclohex-2-en-1-one (5)
(i) Sodium hydroxide solution (10%, 4 ml) was added to a solution of 3-hydroxy-2-propionyl-5-(3-cyanomethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (1.5 g, 4.6 mmol) in toluene (10 ml) and the mixture was refluxed for 2 h. After cooling the toluene was separated and the aqueous layer acidified and extracted with ethylacetate. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated. Chromatography on silica gel (elution with an increasing gradient of ethylacetate in methylene chloride) gave 3-hydroxy-2-propionyl-5-(3-carbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one as a pale solid (0.6 g, 40%). Proton magnetic resonance spectrum (CDCl.sub.3 ; 67 in ppm): 1.25 (3H,t,J6.5 Hz); 2.24 (3H,s); 2.28 (3H,s); 2.32 (3H,s); 2.2-4.2 (7H,m); 3.60 (2H,s); 5.3 (1H,brs); 6.0 (1H,brs); 6.85 (1H,s); 18.10 (1H,s). Infrared spectrum (CHCl.sub.3): .nu. max 1670 b cm.sup.-1. Also recovered from the chromatography was a sodium bicarbonate soluble fraction identified as 2-[3-(4-propionyl-5-hydroxycyclohex-3-one-4-enyl)-2,4,6-trimethylpheny]acetic acid (0.25 g, 17%) a colourless solid. Proton magnetic resonance spectrum (CDCl.sub.3 ; .delta. in ppm): 1.2 (3H, t,J6.5 Hz); 2.13 (3H,s); 2.2 (3H,s); 2.26 (3H, s); 2.3-4.1 (7H,m); 3.50; (2H,s); 6.75 (1H,s). Infrared spectrum: .nu. max (NUjol) 3300-2500 b, 1680-1630 b cm.sup.-1.
(ii) 2-[1-(Ethoxyiminopropyl)-3-hydroxy-5-[3-carbamoylmethyl-2,4,6-trimethylphenyl]cyclohex-2-en-1-one was prepared as described in Example 1 part (iv) from 3-hydroxy-2-propionyl-5-(3-carbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one. The compound was characterized by proton magnetic resonance spectroscopy and the spectroscopic data are recorded in Table 2.
EXAMPLE
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-thiocarbamoylmethyl-2,4,6-trimethylphenyl]cyclohex-2-en-1-one (6)
A solution of 3-hydroxy-2-propionyl-5-(3-cyanomethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (0.77 g, 2.37 mmol) and thioacetamide (0.36 g, 4.74 mmol) in dmf (10 ml) was saturated with anhydrous hydrogen chloride. The solutuion was then heated under a distillation head at 110.degree. for 45 m. Most of the dmf was then distilled off under reduced pressure. The dark red residue was cooled, saturated sodium bicarbonate solution was added, and the aqueous layer extracted with ethylacetate. The organic layer was washed extensively with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure to yield an orange solid. The crude material was purified by chromatography on silica gel (elution with an increasing gradient of ethylacetate in methylene chloride) to give 3-hydroxy-2-propionyl-5-(3-thiocarbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one as a colourless solid (0.40, 47%). Proton magnetic resonance spectrum (CDCl.sub.3 ; .delta. in ppm); 1.15 (3H, t); 2.22 (3H,s); 2.28 (3H,s); 2.36 (3H,s); 2.4-4.2 (9H,m); 6.70 (1H,brs); 6.90 (1H,s); 8.25 (1H,brs); 18.20 (1H,s).
(ii) 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-thiocarbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (6) was prepared as described in Example 1 part (iv). The compound was characterized by proton magnetic resonance spectroscopy and the spectroscopic data are recorded in Table 2.
EXAMPLE 7
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-N,N-dimethycarbamoylmethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (7)
(i) N,N-Dimethyl-(3-formyl-2,4,6-trimethylphenyl) acetic acid amide was prepared by the formylation of N,N-dimethyl mesitylacetic acid amide with dichloromethyl methyl ether using standard conditions.
(ii) 3-hydroxy-2-propionyl-5-(3-N,N-dimethyl carbamoylmethyl -2,4,6-trimethylphenyl) cyclohex-2-en-1-one was prepared from N,N-dimethyl-(3-formyl-2,4,6-trimethylphenyl) acetic acid using standard literature conditions.
(iii) 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(3-N,N-dimethylcarbamoylmethyl-2,4,6-trimethylphenyl) cyclohex-2-en-1-one (7) was prepared using the conditions described in Example 1, part (iv). The compound was characterized by proton magnetic resonance spectroscopy and the data are recorded in Table 2.
EXAMPLE 8
The majority of the compounds of the invention were obtained initially as oils and were characterized by, and can be identified by, their nuclear magnetic resonance spectra. For convenience proton nuclear magnetic resonance (pmr) spectroscopic data is recorded in Table 2 below.
TABLE 2______________________________________Compound Proton Chemical ShiftNo Appearance .about. in ppm (CDCl.sub.3)______________________________________1 Yellow Oil 1.19(3H,t); 1.33(3H,t); 2.23 (3H,s); 2.26(3H,s); 2.46(6H, s); 2.4-4.0(7H,m); 3.67(2H, s); 4.13(2H,q); 15.07(lH, brs).2 Colourless 1.19(3H,t); 1.34(3H,t); solid 2.16(3H,s); 2.26(3H,s); 2.37 (3H,s); 2.47(3H,s); 2.4-4.2 (7H,m); 3.63(2H,s); 4.14 (2H,q); 5.58(1H,brs); 6.34 (1H,brs); 15.02(1H,brs).3 Colourless 1.19(3H,t); 1.34(3H,t); 2.13 solid (3H,s); 2.27(3H,s); 2.34 (3H,s); 2.47(3H,s); 2.94(2H, q); 2.4-4.2(5H,m); 4.13(2H, q); 4.15(2H,s); 6.75(1H, brs); 8.09(1H,brs); 15.15 (1H,brs).4 pale yellow 1.20(3H,t); 1.33(3H,t); 2.34 solid (3H,s); 2.38(3H,s); 2.44(3H, s); 2.4-4.3(5H,m); 2.96(2H, q); 3.64(2H,s); 4.21(2H,q); 6.92(1H,s); 15.00(1H,brs).5 pale solid 1.20(3H,t); 1.33(3H,t); 2.27(3H,s); 2.35(3H,s); 2.38(3H,s); 2.4-4.5(m,9H); 3.61(2H,s); 5.35(1H,brs); 6.0(1H,brs); 6.92(1H,brs).6 pale yellow 1.22(3H,t); 1.37(3H,t); solid 2.28(3H,s); 2.34(3H,s); 2.42(3H,s); 2.6-4.3(5H,m); 2.98(2H,q); 4.17(2H,s); 4.20(2H,q); 6.70(1H,brs); 6.97(1H,s); 8.15(1H,brs); 15.00(1H,brs).7 pale brown 1.19(3H,t); 1.32(3H,t); oil 2.19(3H,s); 2.25(3H,s); 2.35(3H,s); 2.2-4.0(7H,m); 2.98(3H,s); 3.15(3H,s); 3.65(2H,s); 4.12(2H,q); 6.86(1H,s); 14.9(1H,bs).______________________________________
EXAMPLE 9
This non-limiting Example illustrates the preparation of formulations of the compounds of the invention.
(a) Emulsifiable Concentrate
Compound No 4 was dissolved in toluene containing 7% v/v "Teric" N13 and 3% v/v "Kemmat" SC15B to give an emulsifiable concentrate which was diluted with water to the required concentration to give an aqueous emulsion which was applied by spraying.
("Teric" is a Trade Mark and "Teric" N13, is a product of ethoxylation of nonylphenol; "Kemmat" is a Trade Mark and "Kemmat" SC15B is a formulation of calcium dodecylbenzenesulfonate.)
(b) Aqueous Suspension
Compound No 3 (5 parts by weight and "Dyapol" PT (1 part by weight) were added to a 2% aqueous solution (94 parts by weight) of "Teric" N8 and the mixture was ball milled to produce a stable aqueous suspension which may be diluted with water to the required concentration to give an aqueous suspension which may be applied by spraying.
("Dyapol" is a Trade Mark and "Dyapol" PT is an anionic suspending agent; "Teric" N8 is a product of ethoxylation of nonylphenol.)
(c) Emulsifiable Concentrate
Compound No 5 (10 parts by weight), "Teric" N13 (5 parts by weight) and "Kemmat" SC15B (5 parts by weight) were dissolved in "Solvesso" 150 (80 parts by weight) to give an emulsifiable concentrate which may be diluted with water to the required concentration to give an aqueous emulsion which may be applied by spraying.
("Solvesso" is a Trade Mark and "Solvesso" 150 is a high boiling point aromatic petroleum fraction.)
(d) Dispersible Powder
Compound No 1 (10 parts by weight), "Matexil" DA/AC (3 parts by weight), "Aerosol" OT/B (1 part by weight) and china clay 298 (86 parts by weight) were blended and then milled to give a powder composition having a particle size below 50 microns.
("Matexil" is a Trade Mark and "Matexil" DA/AC is the disodium salt of a naphthalenesulfonic acid/formaldehyde condensate; "Aerosol" is a Trade Mark and "Aerosol" OT/B is a formulation of the dioctyl ester of sodium sulfosuccinic acid.)
(e) Dusting Powder
Compound No 1 (10 parts by weight), attapulgite (10 parts by weight) and pyrophyllite (80 parts by weight) were thoroughly blended and then ground in a hammer-mill to produce a powder of particle size less than 200 microns.
Emulsifiable concentrates and/or suspensions of the compounds of the invention were prepared essentially as described in part (a), (b) or (c) above and then diluted with water, optionally containing surface active agent and/or oil, to give aqueous compositions of the required concentration which were used, as described in Examples 10, 11 and 12, in the evaluation of the pre-emergence and post-emergence herbicidal activity of the compounds.
EXAMPLE 10
The pre-emergent herbicidal activity of the compounds of the invention formulated as described in Example 9 was assessed by the following procedure:
The seeds of the test species were sown in rows 2 cm deep in soil contained in seed boxes. The monocotyledonous plants and the dicotyledonous plants were sown in separate boxes and after sowing the two boxes were sprayed with the required quantity of a composition of the invention. Two duplicate seed boxes were prepared in the same manner but were not sprayed with a composition of the invention and were used for comparison purposes. All the boxes were placed in a glass house, lightly watered with an overhead spray to initiate germination and then sub-irrigated as required for optimum plant growth. After three weeks the boxes were removed from the glass house and the effect of the treatment was visually assessed. The results are presented in Table 3 where the damage to plants is rated on a scale of from 0 to 5 where 0 represents from 0 to 10% damage, 1 represents from 11 to 30% damage, 2 represents from 31 to 60% damage, 3 represents from 61 to 80% damage, 4 represents from 81 to 99% damage and 5 represents 100% kill. A dash (-) means that no experiment was carried out.
The names of the test plants are as follows:
______________________________________ Wh Wheat Ot Wild Oats Rg Ryegrass Jm Japanese millet B Barley P Peas Ip Ipomea Ms Mustard Sf Sunflower______________________________________
TABLE 3______________________________________Pre-emergent Herbicidal Activity Appli-Com- cationpound Rate TEST PLANTNo kg/ha Wh Jm Rg Ot B P Ip Ms Sf______________________________________1 1.0 5 5 5 5 5 0 0 0 01 0.25 5 5 5 4 5 -- -- -- --2 1.0 3 5 4 2 2 0 0 0 02 0.25 5 5 5 4 4 -- -- -- --3 1.0 4 5 5 5 5 0 0 0 03 0.25 4 5 5 5 4 -- -- -- --4 1.0 5 5 5 5 5 0 0 0 04 0.25 0 5 5 5 3 -- -- -- --5 1.0 3 5 5 5 4 0 0 0 05 0.25 0 5 4 5 2 -- -- -- --6 1.0 5 5 5 5 4 0 0 0 06 0.25 4 5 5 5 3 -- -- -- --______________________________________
EXAMPLE 11
The post-emergent herbicidal activity of the compounds of the invention formulated as described in Example 9 was assessed by the following procedure.
The seeds of the test species were sown in rows 2 cm deep in soil contained in seed boxes. The monocotyledonous plants and the dicotyledonous plants were sown in separate seed boxes in duplicate. The four seed boxes were placed in a glass house, lightly watered with an overhead spray to initiate germination and then sub-irrigated as required for optimum plant growth. After the plants had grown to a height of about 10 to 12.5 cm one box of each of the monocotyledonous plants and the dicotyledonous plants was removed from the glass house and sprayed with the required quantity of a composition of the invention. After spraying the boxes were returned to the glass house for a further 3 weeks and the effect of treatment was visually assessed by comparison with the untreated controls. The results are presented in Table 4 where the damage to plants is rated on a scale of from 0 to 5 where 0 represents from 0 to 10% damage, 1 represents from 11 to 30% damage, 2 represents from 31 to 60% damage, 3 represents from 61 to 80% damage, 4 represents from 81 to 99% damage and 5 represents 100% kill. A dash (-) means that no experiment was carried out.
The names of the test plants are as follows:
______________________________________ Wh Wheat Ot Wild Oats Rg Ryegrass Jm Japanese millet B Barley P Peas Ip Ipomea Ms Mustard Sf Sunflower______________________________________
TABLE 4______________________________________Post-emergent Herbicidal Activity Appli-Com- cationpound Rate TEST PLANTNo kg/ha Wh Jm Rg Ot B P Ip Ms Sf______________________________________1 0.25 5 5 5 5 5 -- -- -- --1 0.0625 5 5 5 5 5 -- -- -- --2 1.0 5 5 5 5 5 0 0 0 02 0.25 5 5 5 5 5 -- -- -- --2 0.0625 4 5 3 4 4 -- -- -- --3 1.0 5 5 5 5 5 0 0 0 03 0.25 5 5 5 5 5 -- -- -- --3 0.0625 5 5 5 5 5 -- -- -- --4 1.0 5 5 5 5 5 0 0 0 04 0.25 4 5 5 5 5 -- -- -- --4 0.0625 4 5 5 5 4 -- -- -- --5 1.0 5 5 5 5 5 0 0 0 05 0.25 5 5 5 5 5 -- -- -- --5 0.0625 5 5 5 5 5 -- -- -- --6 1.0 5 5 5 5 5 0 0 0 06 0.25 4 5 5 5 5 -- -- -- --6 0.0625 4 5 4 5 5 -- -- -- --7 0.25 5 5 5 5 5 0 0 0 07 0.0625 1 5 4 3 3 -- -- -- --______________________________________
EXAMPLE 12
The compounds were formulated for test by mixing an appropriate amount with 5 ml of an emulsion prepared by diluting 160 ml of a solution containing 21.9 g per liter of "Span" 80 and 78.2 g per liter of "Tween" 20 in methylcyclohexanone to 500 ml with water. "Span" 80 is a Trade Mark for a surface-active agent comprising sorbitan monolaurate. "Tween" 20 is a Trade mark for a surface-active agent comprising a condensate of sorbitan monolaurate with 20 molar proportions of ethylene oxide. Each 5 ml emulsion containing a test compound was then diluted to 40 ml with water and sprayed on to young pot plants (post-emergence test) of the species named in Table 5 below. Damage to test plants was assessed after 14 days on a scale of 0 to 5 where 0 is 0 to 20% damage and 5 is complete kill. The degree of herbicidal damage was assessed by comparison with untreated control plants. The results are given in Table 5 below. A dash (-) means that no experiment was carried out.
The names of the test plants were as follows:
______________________________________Mz MaizeWw Winter wheatRc RiceBr BarleyAv Avena fatuaDg Digitaria sanguinalisAl Alopecurus myosuroidesSt Setaria viridisEc Echinochloa crus-galliSh Sorghum halepenseAg Agropyron repens______________________________________
TABLE 5__________________________________________________________________________Post-emergent Herbicidal Activity Appli-Com- cationpound Rate TEST PLANTNo (kg/ha) Mz Ww Rc Br Av Dg Al St Ec Sh Ag__________________________________________________________________________1 0.1 4 4 2 5 5 4 5 4 5 3 41 0.05 4 3 2 4 4 4 5 4 4 3 32 0.1 4 0 2 3 5 5 4 5 5 3 42 0.05 2 0 0 0 3 5 4 4 4 1 03 0.1 5 4 2 4 5 4 4 4 4 5 43 0.05 0 0 0 2 3 4 4 3 4 3 24 0.1 4 1 4 4 4 4 4 4 4 4 14 0.05 4 0 4 4 4 4 4 4 4 4 15 0.1 4 3 2 4 4 4 4 4 4 4 15 0.05 2 0 0 2 2 3 3 3 4 4 06 0.1 5 4 4 4 5 5 5 5 5 4 56 0.05 4 3 4 4 4 4 5 5 5 4 37 0.1 4 4 4 4 5 4 4 4 5 5 17 0.05 4 0 3 3 1 4 4 3 4 4 0__________________________________________________________________________

Number	Name	Date	Kind
4652303	Watson et al.	Mar 1987
4666510	Watson et al.	May 1987

Herbicidal cyclohexane-1,3-dione derivatives

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