Lubricants comprising novel cyclopentanes, cyclopentadienes, cyclopentenes, and mixtures thereof and methods of manufacture

FIELD OF THE INVENTION
This invention relates to novel hydrocarbyl-substituted cyclopentanes, hydrocarbyl-substituted cyclopentadienes, hydrocarbyl-substituted cyclopentenes, and mixtures thereof, and their use as lubricating compositions, and more particularly, this invention relates to novel hydrocarbyl cyclopentanes, hydrocarbyl cyclopentadienes, hydrocarbyl cyclopentenes, and mixtures thereof, novel methods for formation of the cyclopentadienes and their conversion to the cyclopentenes and cyclopentanes, and use of the cyclopentanes, cyclopentadienes, cyclopentenes and mixtures thereof as lubricating compositions.
BACKGROUND
Cyclopentadiene, cyclopentene and cyclopentane and alkylated derivatives thereof are known in the art. Further, methods are known for preparation of alkylated cyclopentadienes and conversion of these materials to cyclopentenes and cyclopentanes. There is substantial interest in cyclopentadienes, cyclopentenes, and cyclopentanes since cyclopentadiene is characterized by the unique property of being the most acidic aliphatic hydrocarbon known, having a pKa of 18, and also because its reactions as a Diels-Alder diene are extremely facile. Because of the aromaticity of the cyclopentadiene anion (c--C.sub.5 H.sub.5.sup.-), cyclopentadiene is easily the most acidic of the simple hydrocarbons and in fact is comparable in acidity to alcohols. This means that substantial amounts of the anion can be generated with alkoxides and even concentrated solutions of hydroxide. Since it it uniquely stable, it can participate in the carbanion reactions of alkylation, acylation, carboxylation and the like.
U.S. Pat. No. 3,255,267 to Fritz et al relates to the alkylation of cyclopentadienes and discloses the reaction of 1-alkyl or 2-alkyl cyclopentadienes with a primary or secondary alcohol in the presence of an alkaline catalyst to alkylate in either the 1 to 2 position. The 1 isomer may then be further alkylated in either the 3 or 4 position while the 2 isomer can be further alkylated in the 4 position, all of this resulting in the formation of a mixture of isomers. Trialkylated and tetralkylated products are also disclosed. The compounds are described as being capable of epoxidation, polymerization, or for use as intermediates for preparation of other compounds. The alkyl groups added to the cyclopentadiene structure are inclusive of alkyl radicals having 1 to 11 carbon atoms in n-alkyl chains and up to 21 carbon atoms in side chains when the compounds are formed from secondary alcohols and including up to four alkyl substituents on the said cyclopentadiene.
U.S. Pat. No. 3,560,583 discloses cyclopentadiene compounds containing up to five substituents, which substituents can be independently hydrogen, alkyl, aryl or aralkyl. These compounds are prepared by reaction of a cyclopentadiene compound with benzyl halide or allyl halide, an alkali metal hydroxide and a quaternary ammonium salt catalyst.
Polish Pat. No. 55,535 to Makosza, 1968, discloses indene compounds which contain alkyl substituents on the cyclopentadiene portion of the molecule. However, the working examples indicate that only a single alkyl group or two allyl groups are present. U.S. Pat. No. 3,931,334 discloses lubricant compositions which comprise substituted indans, the indan molecule being substituted by methyl and styryl.
In a thesis by Stephen S. Hirsch, University of Maryland, 1963, there is disclosure of base catalyzed alkylation of cyclopentadienes utilizing alcohols to effect the alkylation. Included in this disclosure are alkylation reactions with benzyl alcohol to produce cyclopentadienes which can contain as many as five benzyl substituents. Also disclosed are 1,3-dialkyl indenes.
Polish Pat. No. 55,571 to Makosza discloses cyclopentadienes and processes for preparation of monosubstituted cyclopentadienes by the use of phase-transfer alkylation. The patent is limited to monosubstituted compounds with short chain alkyl groups.
The prior art contains numerous disclosures of methods for the preparation of substituted cyclopentadienes but wherein the substituents usually are short chain alkyl groups. The methods of preparation of such materials vary but do include such processes as the reaction of the cyclopentadiene with alkyl halides in the presence of a base as in U.S. Pat. No. 2,953,607. Similar disclosures may be found in U.S. Pat. Nos. 3,131,227, 4,547,603, 4,567,308, 3,560,583, 4,412,088, and 3,755,492. Of particular interest is 3,131,227 which discloses polysubstituted cyclopentadienes such as pentamethyl and hexamethyl cyclopentadiene which is prepared by a cyclization reaction. Also in Pat. No. 4,567,308, alkyl cyclopentadienes and alkylated derivatives thereof are prepared by the vapor phase reaction of a cyclopentadiene derivative and an aliphatic lower alcohol in the presence of a basic catalyst. These cyclopentadienes and alkylated products are disclosed as being additives for synthetic rubbers, starting materials for resins and/or industrial chemicals.
In a publication by J. Denis, Journal of Synthetic Lubrication, Vol. 1, p. 201-219 (1985), there is disclosure of hydrocarbons which may be used in lubricant compositions. Specifically mentioned in this publication are cycloalkanes and in particular monoalkyl substituted cyclopentanes. This publication is a comparison of various hydrocarbon structures including normal alkanes, alkanes branched by one or more alkyl chains or by a ring, cycloalkanes and aromatics as base stocks for lubricants.
In a publication by Rong et al, Acta Chemica Sinica, Vol. 41, No. 10, October, 1983, pages 971-973 there is disclosure of the use of polyethylene glycol as a phase transfer agent for halide alkylation of cyclopentadiene with alkyl halides. The products produced are monoalkyl substituted cyclopentadienes. In a related article by Rong et al, Journal of Chinese Universities, Vol. 4, page 576-580 (1983), there is disclosure of the synthesis of alkyl substituted derivatives of cyclopentadiene by the phase transfer catalytic reaction of cyclopentadiene with alkyl halides in the presence of potassium hydroxide and polyoxyethylene surfactants as a catalyst. Only monoalkyl substituted cyclopentadienes are prepared.
U.S. Pat. Nos. 3,004,384, 3,356,704, 3,358,008, 3,388,180, 3,391,209, 3,414,626, and 3,419,622 disclose polysubstituted cyclopentadienes and cyclopentanes but wherein the substituent is a short chain alkyl group group or allyl group. Finally, U.S. Pat. Nos. 3,751,500 and 3,636,176 disclose indene compounds which can contain short chain alkyl substituents which are useful as perfume compositions.
In none of the prior art of which Applicants are aware are there disclosures of poly-hydrocarbyl cyclopentanes, cyclopentadienes, cyclopentenes, and mixtures thereof which are useful as lubricant compositions, which useful products may be prepared from novel hydrocarbyl-substituted cyclopentadienes. The present invention provides such novel products as well as methods for their preparation and methods for their use.
SUMMARY OF THE INVENTION
It is accordingly one object of the present invention to provide hydrocarbon-substituted cyclopentanes which are useful as lubricating compositions.
A further object of the invention is to provide novel and useful cyclopentanes which are polyhydrocarbyl substituted and which are prepared from the corresponding hydrocarbyl substituted cyclopentadienes.
A still further object of the present invention is to provide lubricating compositions which contain hydrocarbyl-cyclopentanes as a lubricating component.
There are also provided novel intermediate compositions of matter which comprise hydrocarbyl-substituted cyclopentadienes and hydrocarbyl-substituted cyclopentenes, the cyclopentadienes and cyclopentenes also being useful as lubricating compositions.
Also provided by the present invention are lubricating compositions which comprise novel poly-hydrocarbyl substituted cyclopentadienes and polyhydrocarbyl substituted cyclopentenes.
Also provided by the present invention are lubricating compositions comprising mixtures of hydrocarbyl cyclopentanes, hydrocarbyl cyclopentenes, and/or hydrocarbyl substituted cyclopentadienes, optinally in admixture with a natural lubricant such as mineral oil or other synthetic lubricants as base fluids.
Further provided by the present invention are novel methods for preparation of the hydrocarbon-substituted cyclopentadienes comprising a phase transfer method and an alcohol method.
Other objects and advantages of the present invention will become apparent as the description thereof proceeds.
In satisfaction of the foregoing objects and advantages of the present invention, there is provided as a broad embodiment of the invention, a class of lubricating compositions which comprise one or more hydrocarbyl-substituted cyclopentanes. These hydrocarbyl-substituted cyclopentanes include the individual compounds and mixtures of the hydrocarbyl-substituted cyclopentane compounds. The compounds are of the following general formula: ##STR1## wherein in the above formula, each R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbons, each R.sub.2 is individually and independently selected from hydrocarbyl groups containing about 4 to 36 carbon atoms, z is 0, 1, 2 or 3, and x is an integer ranging from 1 to 6, and x+z cannot be greater than 6. Preferred compounds within this group are those wherein each R.sub.2 is individually and independently selected from alkyl groups having about 8 to 24 carbon atoms, x is an integer of about 2 to 5, and the total number of carbon atoms in the R.sub.2 groups should preferably not exceed about 80.
In a further embodiment of the invention, there are provided novel cyclopentane compositions which are useful as lubricating compositions and which are of the following general formula: ##STR2## wherein each R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbons, each R.sub.2 is individually and independently selected from hydrocarbyl groups having about 4 to 36 carbon atoms, preferably straight or branch chained alkyl groups, z is 0, 1, 2 or 3 and y is an integer ranging from 2 to 6, provided that when at least 2 of the R.sub.2 substituents contain alkyl groups of from 4 to 10 carbon atoms, then y must be an integer of at least 3, y+z cannot be greater than 6. The total number of carbon atoms in the R.sub.2 groups should preferably not exceed about 80.
There are further provided by the present invention novel cyclopentadiene intermediate compounds which can be hydrogenated to the cyclopentanes referred to above, which intermediate cyclopentadienes are of the following general formula: ##STR3## wherein in the above formula, each R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbon atoms, each R.sub.2 is individually and independently selected from hydrocarbyl groups, preferably straight or branch chained alkyl or alkenyl groups of 4 to 36 carbon atoms, z is 0, 1, 2 or 3, and y is an integer of from 2 to 6, and y+z cannot be greater than 6, provided that when up to four of the R.sub.2 groups contain from 4 to 11 carbon atoms, then y must be an integer of at least 5. The total number of carbon atoms in the R.sub.2 groups should preferably not exceed about 80.
The cyclopentadiene compounds of the above formula, referred to as novel intermediate compounds, are also included in a group of novel lubricating compositions. Thus, polyhydrocarbyl substituted cyclopentadienes of the following formula are useful as lubricating compositions: ##STR4## wherein in the above formula, each R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbon atoms, each R.sub.2 is individually and independently selected from hydrocarbyl groups containing about 4 to 36 carbon atoms, z is 0, 1, 2 or 3, and x is an integer ranging from about 1 to 6, and x+z cannot be greater than 6. Preferred compounds within this group are those wherein each R.sub.2 is individually and independently selected from alkyl or alkenyl groups having about 8 to 24 carbon atoms and x is an integer of about 2 to 5, and the total number of carbon atoms in the R.sub.2 groups should preferably not exceed about 80. The cyclopentadienes of this formula may also be used as intermediates for hydrogenation to the cyclopentene and cyclopentane lubricants of the invention.
There are also provided by the present invention lubricating compositions which are partially synthetic lubricants and partially natural lubricants. These lubricating compositions comprise the hydrocarbyl substituted cyclopentanes, or the hydrocarbyl substituted cyclopentadienes, or the hydrocarbyl substituted cyclopentenes, or any mixture thereof, in any proportions with a natural lubricant base such as mineral oil. Also provided are mixtures of the synthetic lubricating compositions of the present invention with other synthetic lubricants so that the resulting lubricating composition is a mixture of synthetic lubricants. Also included within the scope of the invention are mixtures of any or all of the synthetic lubricants of the present invention, alone or in admixture with other synthetic lubricants, or with natural lubricants.
Also provided by the present invention are methods for production of the hydrocarbyl-substituted cyclopentadiene compounds, one method comprising the single step reaction of cyclopentadiene or substituted cyclopentadiene with a molar excess of a hydrocarbylating agent or mixture of such agents of the formula R.sub.2 Y, wherein R.sub.2 is as described above and Y is a leaving group, preferably a halogen, in a reaction vessel containing an aqueous alkaline solution and a phase transfer catalytic agent. In a second method for preparation of the novel cyclopentadienes, cyclopentadiene or substituted cyclopentadiene is reacted with a molar excess of a primary or secondary alcohol or mixture of such alcohols of the formula R.sub.2 OH wherein R.sub.2 is as described above in the presence of a basic catalyst at elevated temperatures, and with removal of water as it is formed, and recovering the product.
DESCRIPTION OF PREFERRED EMBODIMENTS
The present invention is broadly concerned with lubricating compositions which comprise certain hydrocarbyl cyclopentanes, hydrocarbyl cyclopentadienes, hydrocarbyl cyclopentenes, or mixtures thereof, and methods of preparation. The invention is also concerned with a class of novel cyclopentanes and corresponding cyclopentadiene and cyclopentene intermediates, methods for their preparation and methods for conversion of the cyclopentadienes to the cyclopentane lubricants.
In a main embodiment of the invention, novel synthetic fluids which are lubricating compositions comprise a group of polyhydrocarbyl-substituted cyclopentanes of the following formula: ##STR5## wherein in the above formula, each R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbon atoms, each R.sub.2 is individually and independently selected from hydrocarbyl groups containing from about 4 to about 36 carbon atoms and preferably is a straight or branch chained alkyl group of 4 to 36 carbon atoms, z is 0, 1, 2 or 3, and x is an integer ranging from 2 to 6, and x+z cannot be greater than 6.
It will be understood that in Formula I as well as in Formulae II to VIII described hereinafter, that the R.sub.2 hydrocarbon groups can be straight or branch-chained, can be of the same or different chain length, and can contain alicyclic rings of 3 to 7 carbon atoms. Since the cyclopentanes are produced by hydrogenation, little if any unsaturation, except possibly for aromatic double bonds, will remain in the hydrocarbon substituents. In the definition of R.sub.1 in the Formula I compounds, as well as the compounds of Formulae II to VIII described hereinafter, it will be understood that the alkyl groups may be the same or different and straight or branch-chained.
These hydrocarbon substituted cyclopentanes have been found to provide excellent lubricating characteristics which make them useful as lubricants in internal combustion engines and in other areas where good lubricity is a requirement. The lubricants may comprise individual hydrocarbyl-substituted cyclopentanes or mixtures thereof. The compounds provide the appropriate specific gravity, refractive indicies, viscosities, and low and high temperature characteristics which are required for an outstanding lubricant. In particular the lubricants exhibit specific gravities ranging from about 0.835 to about 0.860; refractive indices ranging from about n.sub.D.sup.25 C 1.450 to 1.40; viscosities at 100.degree. C. (cSt) ranging from 2.0 to 20.0, at 40.degree. C. (cST) ranging from 6.0 to 350, at 0.degree. C. (cP) ranging from 200 to 13,000, and at -40.degree. C. (cP), ranging from 1500 to 600,000. The viscosity index ranges from 45 to 200. The compositions also provide excellent low temperature pour points. Flash points range from 500.degree. to 600.degree. F. and fire points range from 500 to 650 with minimum loss to evaporation at these temperatures.
In the hydrocarbon substituted cyclopentane compositions described above, some compounds of the above formula which contain a single methyl group substituent provide lubricants which have a lowered pour point as compared to otherwise comparable cyclopentanes. This causes the cyclopentanes to be particularly useful in certain lubricating environments.
A preferred group of hydrocarbon substituted cyclopentane lubricants are those wherein x is an integer of 3 to 5, R.sub.1 is methyl and z is 0 or 1, and R.sub.2 is an alkyl group of 8 to 24 carbon atoms, and wherein x is an integer of 2 to 4, R.sub.1 is methyl and z is 0 or 1, and R.sub.2 is an alkyl group of 13 to 24 carbon atoms.
In further embodiments of the invention, the intermediate hydrocarbon-substituted cyclopentadienes and hydrocarbon substituted cyclopentenes are also provided as lubricating compositions. These compounds have lubricating characteristics including viscosities and pour points which make them useful in a variety of areas.
The lubricating compositions which comprise cyclopentadienes are of the following formula: ##STR6## wherein z, R.sub.1 and R.sub.2 are as defined above in Formula I and x is an integer ranging from 1 to 6.
Also provided by the present invention are cyclopentene compositions which are useful as synthetic lubricants. These cyclopentenes may be described by the following general formula: ##STR7## wherein R.sub.1, R.sub.2, z and and x are as defined above.
There is also provided by the present invention partial synthetic lubricant compositions in which the hydrocarbon-substituted cyclopentanes, the hydrocarbon-substituted cyclopentenes, or the hydrocarbon-substituted cyclopentadienes, used either alone or in admixture, are mixed with a natural base fluid such as mineral oil to form the lubricant. Compositions of this type may contain about 10 to 90% of any of the synthetic lubricants of this invention mixed with 90 to 10% of a mineral oil base fluid. Compositions of this type show enhanced lubricant properties.
In a further embodiment of the invention, mixtures of the hydrocarbon-substituted cyclopentanes, the hydrocarbon-substituted cyclopentenes, or the hydrocarbon-substituted cyclopentadienes, used either alone or in admixture, may be mixed with other synthetic lubricants such as poly-alpha-olefins, esters and polyol esters. These mixtures may include 10 to 90% of the synthetic hydrocarbon substituted cyclopentanes, cyclopentenes, and/or cyclopentadienes of this invention, mixed with 90 to 10% of any other compatible synthetic lubricant.
In a still further embodiment of the invention, lubricating compositions are provided which comprise mixtures of the hydrocarbon-substituted cyclopentanes, hydrocarbon-substituted cyclopentenes, and hydrocarbon-substituted cyclopentadienes of this invention, the mixtures being in varying and all proportions. Mixtures of this type arise from incomplete hydrogenation in production of the cyclopentanes from the cyclopentadienes as described hereinafter. This hydrogenated mixture will comprise mixtures of these compounds which can be used as such as a lubricating composition.
Preferred lubricating compositions according to the invention are those cyclopentanes, cyclopentenes and cyclopentadienes which contain a plurality of R.sub.2 hydrocarbyl groups, i.e., wherein x is 3 to 6. Even more preferred are those compounds wherein the R.sub.2 substituents are hydrocarbyl groups of different carbon chain length.
In a further embodiment of the invention, there are also provided a group of novel hydrocarbyl substituted cyclopentanes which are of the following formula: ##STR8## wherein in the above formula, R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbon atoms, R.sub.2 is individually and independently selected from hydrocarbyl groups of 4 to 36 carbon atoms, and preferably are straight or branch chained alkyl groups containing 4 to 36 carbon atoms which can contain alicyclic rings of 3 to 7 carbon atoms, z is 0, 1, 2 or 3, and y is an integer of from 2 to 6, provided that when at least two of the R.sub.2 groups are carbon chains of from about 4 to 10 carbon atoms, then the integer y must be at least 3, and y+z cannot be greater than 6.
The hydrocarbon-substituted cyclopentanes of the present invention are prepared by hydrogenation of the corresponding hydrocarbon-substituted cyclopentadienes by conventional hydrogenation techniques. The hydrogenation reactions of this type are known in the art and generally comprise reaction of the hydrocarbon-substituted cyclopentadiene intermediate or mixture of intermediates in the presence of a hydrogenation catalyst such as Raney nickel or palladium and in the presence or absence of an organic solvent such as an aliphatic hydrocarbon. In carrying out the hydrogenation reaction, the reactor is pressurized with hydrogen to a pressure which may range up to about 3000 psi and heated in the range of 75.degree. to 200.degree. C. until the hydrogenation is complete as evidenced by cessation of hydrogen uptake. On removal of the catalyst and solvent, the hydrogenated cyclopentane is recovered.
The hydrocarbon-substituted cyclopentadienes which serve as precursors, many of which are also novel compounds, may be characterized by the following general formula: ##STR9## In the above formula, R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbon atoms, R.sub.2 is individually and independently selected from hydrocarbon substituents of 4 to 36 carbon atoms, preferably straight or branch-chained alkyl groups, alkenyl groups, or alkynyl groups having from 4 to 36 carbon atoms which can contain alicyclic rings of 3 to 7 carbons and/or aromatic rings of 6 to 12 carbon atoms, z is 0, 1, 2, or 3, x+z cannot be greater than 6, and x is an integer ranging from 1 to 6. It is preferred that at least two of the R.sub.2 groups contain from 8 to 13 carbon atoms, and that x be an integer of 3 to 5.
A novel group of cyclopentadiene compounds are those of the formula: ##STR10## wherein z, R.sub.1 and R.sub.2 are as defined above, and y is an integer of 2 to 6, and y+z cannot be greater than 6, provided that when up to four of the R.sub.2 groups contain from 4 to 11 carbon atoms, then y is an integer of at least 5.
The intermediate hydrocarbon-substituted cyclopentenes, most of which are also novel compounds, may be characterized by the following general formula: ##STR11## In the above formula, R.sub.1 is individually and independently selected from alkyl groups of 1 to 4 carbon atoms, R.sub.2 is individually and independently selected from hydrocarbon substituents of 4 to 36 carbon atoms, preferably straight or branch-chained alkyl groups having from 4 to 36 carbon atoms which can contain alicyclic rings of 3 to 7 carbons and/or aromatic rings of 6 to 12 carbons, z is 0, 1, 2 or 3, and x is an integer ranging from 1 to 6, and x+z cannot be greater than 6. It is preferred that at least two of the R.sub.2 groups contain from 4 to 10 carbon atoms, and that x be an integer of 3 to 5. A preferred group of compounds includes those wherein the R.sub.2 groups contain from 8 to 12 carbon atoms and x is 3 to 5.
A novel group of cyclopentene compounds are those of the formula: ##STR12## wherein z, R.sub.1 and R.sub.2 are as defined above, and y is an integer of 2 to 6, provided that when at least two of the R.sub.2 groups contain from 4 to 10 carbon atoms then y is an integer of at least 3. In a particularly preferred group, when R.sub.2 is an alkyl group which contains from 4 to 10 carbon atoms, then the integer x is 3, 4 or 5, the latter particularly representing a group of novel cyclopentene intermediates.
In the cyclopentanes, cyclopentenes and cyclopentadienes of the invention, the total number of carbon atoms in the R.sub.2 substituents should preferably not exceed about 80.
Preferred compounds or mixtures of compounds according to the invention include cyclopentane, cyclopentadiene, and cyclopentene lubricants which, with reference to Formulae I, II, and III, may be defined as follows:
(1)
z=0;
x=3 or 4;
R.sub.2 =C.sub.8 and/or C.sub.10 alkyl hydrocarbon.
(2)
z=0;
x=3 or 4;
R.sub.2 =C.sub.9 and/or C.sub.10 and/or C.sub.11 alkyl hydrocarbon.
(3)
z=0;
x=3 or 4; `R.sub.2 =C.sub.12 and/or C.sub.13 alkyl hydrocarbon.
(4)
z=0;
x=2 or 3;
R.sub.2 =2-octyl-1-dodecyl
Particularly preferred specific classes of compounds and specific compounds or mixtures which are also useful as lubricants include the following:
Cyclopentanes
Tri-n-octyl cyclopentane
Tetra-n-octyl cyclopentane
Penta-n-octyl cyclopentane
Tri-n-nonyl cyclopentane
Tetra-n-nonyl cyclopentane
Penta-n-nonyl cyclopentane
Tri-n-decyl cyclopentane
Tetra-n-decyl cyclopentane
Penta-n-decyl cyclopentane
Tri-n-undecyl cyclopentane
Tetra-n-undecyl cyclopentane
Penta-n-undecyl cyclopentane
Tri-n-dodecyl cyclopentane
Tetra-n-dodecyl cyclopentane
Penta-n-dodecyl cyclopentane
Tri-2-ethylhexyl cyclopentane
Tetra-2-ethylhexyl cyclopentane
Di-n-octyl, n-decyl cyclopentane
n-octyl, di-n-decyl cyclopentane
Trioctyl, n-decyl cyclopentane
Di-n-octyl, di-n-decyl cyclopentane
n-octyl, tri-n-decyl cyclopentane
Tri-n-tridecyl cyclopentane
Tetra-n-tridecyl cyclopentane
Penta-n-tridecyl cyclopentane
Cyclopentenes
Tri-n-octyl cyclopentene
Tetra-n-octyl cyclopentene
Penta-n-octyl cyclopentene
Tri-n-nonyl cyclopentene
Tetra-n-nonyl cyclopentene
Penta-n-nonyl cyclopentene
Tri-n-decyl cyclopentene
Tetra-n-decyl cyclopentene
Penta-n-decyl cyclopentene
Tri-n-undecyl cyclopentene
Tetra-n-undecyl cyclopentene
Penta-n-undecyl cyclopentene
Tri-n-dodecyl cyclopentene
Tetra-n-dodecyl cyclopentene
Penta-n-dodecyl cyclopentene
Tri-2-ethylhexyl cyclopentene
Tetra-2-ethylhexyl cyclopentene
Di-n-octyl, n-decyl cyclopentene
n-octyl, di-n-decyl cyclopentene
Trioctyl, n-decyl cyclopentene
Di-n-octyl, di-n-decyl cyclopentene
n-octyl, tri-n-decyl cyclopentene
Tri-n-tridecyl cyclopentene
Tetra-n-tridecyl cyclopentene
Penta-n-tridecyl cyclopentene
Cyclopentadienes
Tri-dodecyl cyclopentadiene
Tetra-dodecyl cyclopentadiene
Penta-dodecyl cyclopentadiene `Penta-n-butyl cyclopentadiene
Penta-n-octyl cyclopentadiene
Penta-n-nonyl cyclopentadiene
Penta-n-decyl cyclopentadiene
Di-n-octyl, n-decyl cyclopentadiene
n-octyl, di-n-decyl cyclopentadiene
Trioctyl, n-decyl cyclopentadiene
Di-n-octyl, di-n-decyl cyclopentadiene
n-octyl, tri-n-decyl cyclopentadiene
Tri-n-tridecyl cyclopentadiene
Tetra-n-tridecyl cyclopentadiene
Penta-n-tridecyl cyclopentadiene
The hydrocarbyl substituted cyclopentadiene intermediates of the invention are prepared using a hydrocarbylating or phase transfer preparation method or an alcohol preparation method. In the phase transfer method, cyclopentadiene or substituted cyclopentadiene and an alkylating agent such as alkyl halide or mixture of alkyl halides are added to a reaction vessel containing an alkaline aqueous solution and further containing a phase transfer catalytic agent. The alkylating agent is used in a molar excess depending on the amount of alkyl substitution desired. The preferred alkylating agent is an alkyl halide of the formula, R.sub.2 Y wherein R.sub.2 is as described above and Y is a leaving group, preferably Cl or Br, and the process is described herein with reference to this reaction. It is preferred that about 3 to 6 moles of alkyl halide should be used per mole of cyclopentadiene. The alkaline aqueous solution will comprise sodium hydroxide or potassium hydroxide in preferred embodiments. The mixture of cyclopentadiene, alkyl halide, catalyst and alkali is permitted to react in aqueous solution with vigorous stirring for a period of from about 1/2 to 10 hours. On completion of the reaction, and cessation of agitation, two phases will form, an organic phase and a water phase. The product will be contained in the organic phase and may be recovered by conventional methods as by separation of phases and recovery.
It is sometimes desirable to add an organic solvent or water or both to facilitate separation of the two phases. In a preferred procedure, the organic layer is removed and any excess alkyl halide and/or solvent removed to provide the alkylated cyclopentadiene which can be used for conversion to the cyclopentane without further purification. This is a single step reaction which provides good yields of the substituted cyclopentadiene.
In conducting the hydrocarbylation reaction by the phase transfer method, the preferred temperature range is from about -20.degree. to 120.degree. C. with a residence time or reaction time of from 1/2 hour up to 3 days. The molar ratio of alkyl halide to cyclopentadiene should range from about 1:1 up to about 20:1. The ratio of alkali metal hydroxide to cyclopentadiene reactant in this reaction may range from 1:1 up to 50:1.
Suitable phase transfer catalysts include n-alkyl (C.sub.12 -C.sub.16) dimethylbenzylammonium chloride, sold commercially as Hyamine 3500, triethylbenzylammonium chloride, sold commercially as TEBAC, a mixture of methyl trialkyl (C.sub.8 -C.sub.10) ammonium chlorides, sold commercially as Adogen.RTM. 464, polyethylene glycols and polyethers.
In a separate method for preparation of the hydrocarbon-substituted cyclopentadienes, an alcohol or mixture of alcohols of the formula R.sub.2 OH wherein R.sub.2 is as described above, is combined with a basic catalyst such as an alkali metal hydroxide or alkoxide in a reaction vessel. The alcohol reactant or mixture of alcohols is a primary or secondary alcohol and is used in sufficient amounts to provide a molar excess of about 3 to 6 moles. The cyclopentadiene or hydrocarbon-substituted cyclopentadiene is then added to the reaction vessel at room temperature or a temperature as high as the reflux temperature of the mixture, which would be at about the boiling temperature of the alcohol(s) being used. Alternatively, a portion of the cyclopentadiene may be mixed with the alcohol and alkali in the reactor and the remaining cyclopentadiene added to the reaction mixture over a period of time as the reaction proceeds. An inert solvent may also be included if necessary depending on the alcohol reactants. Further, the reaction may be carried out in a closed container so that higher temperatures in excess of 180.degree., and up to 260.degree. C. can be reached using lower boiling alcohols. As the reaction proceeds, water will be produced and is removed as it is formed. On completion of the reaction, the mixture is allowed to cool and then mixed with water or poured onto ice and two layers allowed to separate. The organic and aqueous layers are separated using an organic solvent to aid the separation if necessary. After removal of excess alcohol and any solvent from the organic layer, the polyalkyl cycopentadiene is recovered.
In an alternative work-up procedure, the reaction mixture may be filtered. The alcohol may be separated by distillation before or after filtration.
It was unexpected that high yields of polyalkylated products from alcohols, including long chain alcohols, could be obtained from this reaction without the use of high pressure.
In conducting the hydrocarbylation by the alcohol method, minor side products may be formed. For example, the acid corresponding to the alcohol and a dimeric alcohol may also be formed. The careful exclusion of oxygen and careful adjustment of the alcohol to base ratios aid in suppression of the formation of these byproducts. If secondary alcohols are used, the byproducts are less significant.
The alcohol alkylation is preferably carried out in the temperature range of 180.degree.-300.degree. C. for a reaction time which may range from 10 minutes to 3 days. The mole ratio of alcohol to cyclopentadiene may range from 1:1 up to 50:1 and the ratio of alkali metal hydroxide or alkoxide to cyclopentadiene reactant may range from 0.1:1 up to 10:1.
The precursor cyclopentadienes to be reacted by the phase transfer method or alcohol method are preferably those set forth in Formula V above except that in such case, x can be 0, and x+z must be 0, 1, 2, 3, 4 or 5 in the phase transfer method, and x+z must be 0, 1, 2, 3 or 4 in the alcohol method. For example the R.sub.1 and/or R.sub.2 hydrocarbyl groups could be added stepwise depending on the amount of hydrocarbylating agent used. The final products and precursor compounds as described are considered to be inclusive of all such compounds.
The cyclopentene intermediates of this invention are produced by partial or incomplete hydrogenation of the cyclopentadienes when preparing the cyclopentanes. This hydrogenation reaction if carried to completion will produce the cyclopentanes described above. However, incomplete hydrogenation will result in production of at least some cyclopentenes and usually a mixture of the hydrocarbon substituted cyclopentenes and cyclopentanes. Some starting cyclopentadienes which are not hydrogenated may also remain in the mixture. Thus, the hydrogenation reaction can produce a variety of mixtures of products as well as the cyclopentenes and the cyclopentanes of the invention.

The following examples are presented to illustrate the invention but the invention is not to be considered as limited thereto. In the examples and throughout the specification, parts are by weight unless otherwise indicated.
EXAMPLE 1
Preparation of Di(n-octyl)cyclopentadienes (Phase Transfer Method)
Cyclopentadiene (99 g, 1.5 moles), and n-octyl bromide (476 g, 3.2 moles), were added to a 5-liter reaction flask, containing an aqueous 56 percent potassium hydroxide solution (1950 ml, 30 moles KOH) and a catalytic amount of Adogen.RTM. 464 (25 g), cooled in an ice bath. The mixture was stirred vigorously for 30 minutes in the ice bath, then the bath was removed. The mixture was stirred for an additional 3 hours, while warming to room temperature. The layers were separated, water and pentane being added to facilitate workup, and the organic phase was washed with water until neutral. The organic layer was dried over MgSO.sub.4 and the pentane removed in vacuo, affording 372 g crude yield.
Gas chromatographic analysis provided the following analysis (86.5% total yield):
mono(n-octyl)cyclopentadienes 15.2%, 56.5 g, 0.317 moles (21.1% yield)
di(n-octyl)cyclopentadienes 75.7%, 281.6 g, 0.971 moles (64.7% yield);
tri(n-octyl)cyclopentadienes 1.1%, 4.1 g, 0.010 moles (0.6% yield).
EXAMPLE 2
Preparation of tri/tetra(n-decyl)cyclopentadienes (Phase Transfer Method)
Cyclopentadiene (23 g, 0.35 moles), and n-decyl bromide (300 g, 1.36 moles), were added to a 2-liter reaction flask containing an aqueous 56 percent potassium hydroxide solution (500 ml, 7.5 moles KOH) and a catalytic amount of Adogen.RTM. 464 (13 g), in a water bath at room temperature. The mixture was vigorously stirred for one hour then heated, with continuing stirring for 41/4 hours at 100.degree. C. After cooling, the layers were separated, water and heptane added to facilitate workup, and the organic phase was washed with water until neutral. The organic phase was dried over MgSO.sub.4 and the solvent removed in vacuo, affording 247 g crude yield. Unreacted n-decyl bromide (40 g, 0.18 mole) was distilled off to give a pot residue (200 g) of product.
Gas chromatographic analysis provided the following analysis (98.6% total yield):
di(n-decyl)ether 3.4%, 6.8 g, 0.023 moles;
di(n-decyl)cyclopentadienes 0.8%, 1.6 g, 0.005 moles (1.4% yield);
tri(n-decyl)cyclopentadienes 41.2%, 82.4 g, 0.170 moles (48.6% yield);
tetra(n-decyl)cyclopentadienes 53.3%, 106.6 g, 0.170 moles (48.6% yield).
EXAMPLE 3
Preparation of Isodecylcyclopentanes (Alcohol method)
Isodecanol (420 g, 2.65 moles) and solid potassium hydroxide (87%, 10.3 g, 0.16 moles KOH) were mixed in a 1-liter reaction flask fitted with a mechanical stirrer, a dropping funnel, a Dean-Stark trap with condenser, a thermometer and a serum capped sampling port. Prior to heating, a portion of the dicyclopentadiene (6.6 g, 0.05 moles) was added to the reaction mixture. The flask was then heated to 200.degree. C. After water began collecting in the Dean-Stark trap, the remaining dicyclopentadiene (28.4 g, 0.22 moles) was added dropwise over a 1.5 hour period. The reaction mixture was heated for 4 hours after the completion of the dicyclopentadiene addition. The temperature rose to 245.degree. C. over the course of the reaction. After cooling, the reaction mixture was poured into water. Hexane was added to facilitate workup. The layers were separated. The aqueous layer was saved for further workup. The organic phase was washed with water until neutral. The organics were dried over MgSO.sub.4 and the solvent removed in vacuo. The organic concentrate was carried through the hydrogenation affording 387 g.
Gas chromatographic analysis provided the following analysis (80% total yield):
isodecanol 25.4%, 98.3 g, 0.621 moles;
isoeicosanol 2.9%, 11.2 g, 0.0380 moles;
tri(isodecyl)cyclopentanes 7.0%, 27.1 g, 0.056 moles (11% yield);
tetra(isodecyl)cyclopentanes 48.1%, 186.1 g, 0.297 moles (56% yield;
penta(isodecyl)cyclopentanes 13.0%, 50.3 g, 0.066 moles (13% yield).
The aqueous layer was acidified with hydrochloric acid and extracted with ether. The layers were separated and the organic layer washed with water until neutral. The organics were dried over MgSO.sub.4 and the solvent removed in vacuo, affording isodecanoic acid (23.4 g, 0.136 moles). Of the 2.65 moles of isodecanol used, 2.52 moles (95%) are accounted for.
EXAMPLE 4
Hydrogenation of tri(n-decyl)cyclopentadienes
A 4-liter autoclave was charged with the crude alkylcyclopentadienes (159 g; di(n-decyl)cyclopentadienes, 34.7 g, 21.8%; tri(n-decyl)cyclopentadienes, 117.2 g, 73.7%; and tetra(n-decyl)cyclopentadienes 2.2 g, 1.4%), (prepared as in Example 2) 10% palladium on activated carbon (4 gms), and heptane (500 ml) to facilitate stirring. The vessel was pressurized to 500 psi of hydrogen and heated at 125.degree. C. for 19 hours with stirring. After cooling, the vessel pressure was 350 psi. The catalyst was filtered and the solvent removed in vacuo affording 150 g of clear colorless oil with a bromine number of zero.
EXAMPLE 5
Using the procedures of Examples 1, 2 and 3, the cyclopentadiene derivatives set forth in the following Table 1 were prepared. The table indicates the preparative method used.
TABLE 1______________________________________CYCLOPENTADIENE DERIVATIVE ##STR13## For- Meth- x =R.sub.2 mula Class.sup.a od.sup.b 2 3 4 5 6______________________________________n-butyl C.sub.4 H.sub.9 1.degree. P X X X X Xn-hexyl C.sub.6 H.sub.13 1.degree. P X X X X Xn-octyl C.sub.8 H.sub.17 1.degree. P, A X X X Xn-decyl C.sub.10 H.sub.21 1.degree. P, A X X X Xn-dodecyl C.sub.12 H.sub.25 1.degree. P, A X X X Xn-tetradecyl C.sub.14 H.sub.29 1.degree. P X X Xisodecyl C.sub.10 H.sub.21 1.degree. A X X X Xisotridecyl C.sub.13 H.sub.27 1.degree. A X X X X2-ethyl-1-hexyl C.sub.8 H.sub.17 1.degree. P, A X X X2-octyl-1-dodecyl C.sub.20 H.sub.41 1.degree. A X X2-decyl-1- C.sub.24 H.sub.49 1.degree. A X Xtetradecyl2-octyl C.sub.8 H.sub.17 2.degree. P, A X Xt-butyl C.sub.4 H.sub.9 3.degree. P X X______________________________________ .sup.a 1.degree. = primary alkyl; 2.degree. = secondary alkyl; 3.degree. tertiary alkyl .sup.b P = Phase Transfer method; A = Alcohol method
EXAMPLE 6
Using the procedures of Examples 1, 2 and 3, the methylcyclopentadienes set forth in the following Table 2 were prepared. The preparative method is indicated.
TABLE 2______________________________________METHYLCYCLOPENTADIENE ##STR14## x =R.sub.2 Formula Class.sup.a Method.sup.b 2 3 4 5______________________________________n-octyl C.sub.8 H.sub.17 1.degree. A X X Xn-decyl C.sub.10 H.sub.21 1.degree. A, P X X Xn-dodecyl C.sub.12 H.sub.25 1.degree. A X X Xisodecyl C.sub.10 H.sub.21 1.degree. A X X X______________________________________ .sup.a 1.degree. = primary alkyl .sup.b P = Primary Transfer method; A = Alcohol method
EXAMPLE 7
Using the hydrogenation procedures of Example 4, the alkyl substituted cyclopentanes of Table 3 were prepared. The column indicating "Class" designates a straight or branch chained substituent.
TABLE 3______________________________________CYCLOPENTANE DERIVATIVES ##STR15## x =R.sub.2 Formula Class.sup.a 2 3 4 5______________________________________n-octyl C.sub.8 H.sub.17 1.degree. X X X Xn-decyl C.sub.10 H.sub.21 1.degree. X X X Xn-dodecyl C.sub.12 H.sub.25 1.degree. X X X Xisodecyl C.sub.10 H.sub.21 1.degree. X X X Xisotridecyl C.sub.13 H.sub.27 1.degree. X X X X2-ethyl-1-hexyl C.sub.8 H.sub.17 1.degree. X X X2-octyl-1-dodecyl C.sub.20 H.sub.41 1.degree. X X2-decyl-1-tetradecyl C.sub.24 H.sub.49 1.degree. X X2-octyl C.sub.8 H.sub.17 2.degree. X X______________________________________ .sup.a 1.degree. = primary alcohol; 2.degree. = secondary alcohol
EXAMPLE 8
Using the hydrogenation procedures of Example 4, the substituted methylcyclopentanes of Table 4 were prepared. The column indicating "Class" designates a straight or branch chained substituent.
TABLE 4______________________________________METHYLCYCLOPENTANE DERIVATIVES ##STR16## x =R.sub.2 FORMULA CLASS 2 3 4______________________________________n-octyl C.sub.8 H.sub.17 1.degree. X X Xn-decyl C.sub.10 H.sub.21 1.degree. X X Xn-dodecyl C.sub.12 H.sub.25 1.degree. X X Xisodecyl C.sub.10 H.sub.21 1.degree. X X X______________________________________
EXAMPLE 9
Chemical Identification
Chemical characterization of alkylcyclopentadienes and alkylcyclopentanes was by infrared spectroscopy (IR), nuclear magnetic resonance spectrometry (NMR) and gas chromatography (GC), especially in conjunction with mass spectrometry (GC-MS). A few examples were meticulously examined and structures of products determined and then quantitative analysis and further identification was made by analogy to these carefully characterized samples.
Interpretation of Spectroscopic Data Mass Spectrometry
Alkylcyclopentadienes (see Table 5 following)--A detailed analysis of n-butyl cyclopentadienes showed that the parent peak was prominent enough to be recognizable. Common fragments were P-43(minus n-propyl), P-57(minus n-butyl), P-98(minus propene and butene), P-99(minus n-propyl and n-butene) and 57(n-butyl). Other cyclopentadienes also gave parent peaks prominent enough to allow assignment to be made on that basis alone.
Alkylcycopentanes--Mass spectra are very similar to other saturated hydrocarbons except that the parent is C.sub.n H.sub.2n.
Infrared Spectroscopy
Alkylcyclopentanes (See Table 6 following)--The IR spectra are indistinguishable from other saturated hydrocarbons with alkyl components; e.g., hydrogenated 1-decene oligomers. Bands are at 2960 cm.sup.-1, 2850 cm.sup.1 (H-C(sp.sup.3) stretch); 1460 cm.sup.-1, 1375 cm.sup.-1, (H-C(sp.sup.3) bend) and 720 cm.sup.-1 (--(CH.sub.2).sub.x -- rock, x>4).
Alkylcyclopentadienes (See Table 6)--In addition to the bands found in the alkylcyclopentanes, bands for unsaturation are found at 3050 cm.sup.-1 (H-C(sp.sup.2) stretch, 1650 and 1620 (C=C stretch), 970 and 890 (H--C(sp.sup.2) bend).
Nuclear Magnetic Resonance Spectrometry
Alkylcyclopentanes--Both .sup.1 H and .sup.13 C NMR Spectra are dominated by n-alkyl resonances: (1) .sup.1 H NMR, CH.sub.3 at 0.9 ppm, CH.sub.2 at 1.3 ppm, CH at 1.5; (2) .sup.13 C NMR, CH.sub.3 --14.2 ppm, CH.sub.2 's at 22.8 ppm, 29.7 ppm, 32.0 ppm and CH's clustered about 40 ppm.
Alkylcyclopentadienes--In addition to the resonance of alkylcyclopentanes due to the alkyl groups, unsaturation leads to resonances at 5.80 and 6.20 ppm in the .sup.1 H spectrum for protons on sp.sup.2 carbon and 2.35 and 2.8 for allylic and bis-allylic CH.sub.2 's respectively. Similarly, resonances due to unsaturation are observed in the 150.0 to 110.00 ppm region for sp.sup.2 carbons and 45.0 to 35.0 ppm region for allylic carbons in the .sup.13 C spectra of alkylcyclopentadienes.
TABLE 5__________________________________________________________________________Mass Spectral Data for Alkyl CyclopentadienesGC - Mass Spec of C.sub.5 (R.sub.2).sub.x H.sub.6-x, R.sub.2 = n-butylRetention INTENSITY (% OF BASE PEAK) Time* P (Parent) P-43 P-56 P-57 P-71 P-85 P-88 P-99 57X (Minutes) M.sup.+ --C.sub.3 H.sub.7 --C.sub.4 H.sub.8 --C.sub.4 H.sub.9 --C.sub.5 H.sub.11 --C.sub.6 H.sub.13 --C.sub.7 H.sub.14 --C.sub.7 H.sub.14 C.sub.4 H.sub.9__________________________________________________________________________2 20.4 24 45 0 42 24 95 63 100 403 29.4 18 53 55 18 53 19 40 100 603 29.5 18 33 3 16 62 17 27 100 533 32.1 27 100 2 12 10 42 40 42 244 35.8 9 52 3 10 0 8 29 27 1004 36.1 22 100 12 23 2 12 47 50 884 36.5 25 100 10 25 2 12 47 38 864 37.2 17 22 88 18 1 7 47 100 624 37.9 30 100 8 20 3 12 35 42 564 38.3 7 <1 18 100 0 1 <1 3 165 40.8 32 79 23 19 0 5 14 38 1005 41.4 45 100 23 19 1 6 27 35 675 42.2 5 <1 26 100 0 0 2 2 176 45.5 100 89 32 30 0 2 10 38 37__________________________________________________________________________
TABLE 6______________________________________Infrared Spectra of Representative Alkylcyclopentadienesand AlkylcyclopentanesDi(n-decyl)cyclopentadienes andDi(n-decyl)cyclopentanes.Frequency, .about..nu. ##STR17## ##STR18## Assignment______________________________________3044 cm.sup.-1 sp.sup.2 CH stretch2960 2960 sp.sup.3 CH stretch2850 2850 sp.sup.3 CH stretch1653 c = c stretch1622 c = c stretch1560 c = c stretch1465 1465 CH.sub.2 bending1375 1375 CH.sub.3 bending968 sp.sup.2 CH bend891 sp.sup.2 CH bend721 721 (CH.sub.2).sub.x x > 4, rocking______________________________________
EXAMPLE 10
To evaluate the alkyl cyclopentanes for lubricating properties, tests were carried out to measure physical properties which are relevant to use as a synthetic lubricant. Set forth in the following Table 7 are specific gravity values of the indicated cyclopentanes, in Table 8 are set forth refractive index values of the indicated cyclopentanes, in Table 9 are set forth viscometric properties of the indicated alkylcyclopentanes; in Table 10 are low temperature properties of the indicated alkylcyclopentanes; and set forth in Table 11 are high temperature properties of the indicated alkylcyclopentanes.
TABLE 7______________________________________Specific Gravity of Representative Alkylcyclopentanes ##STR19## X =Sample # R.sub.1 R.sub.2 2 3 4 5 S.G.______________________________________1 H (n-decyl) -- 100% -- -- 0.83682 H (n-octyl) -- 13 100% -- 0.83683 H (n-decyl) -- 20% 70% 10% 0.84304 H (n-decyl) -- -- 67% 33% 0.84505 H (n-dodecyl) -- 40% 60% -- 0.8509______________________________________
TABLE 8______________________________________Refractive Indexes of Representative Alkylcyclopentanes ##STR20##Sam-ple X =# R.sub.1 R.sub.2 2 3 4 5 n.sub.D.sup.25.degree.______________________________________ C.1 H n-octyl -- 100% -- -- 1.45732 H n-decyl -- 100% -- -- 1.46043 H/Me = n-decyl -- 100% -- -- 1.4612 1/14 H n-octyl -- -- 100% -- 1.46125 Me n-octyl -- 40% 60% -- 1.46306 H n-decyl -- 30% 65% 5% 1.46367 H n-decyl -- -- 67% 33% 1.46548 H n-dodecyl -- 40% 60% 1.46479 H isodecyl 1.4672______________________________________
TABLE 9__________________________________________________________________________Viscometric Properties of Representative Alkylcyclopentanes ##STR21## Viscosity X = 100.degree. C. 40.degree. C. 0.degree. C. -40.degree. C. Viscosity.sup.cSample # R.sub.1 R.sub.2 2 3 4 5 (cSt).sup.a (cSt).sup.a (cP).sup.b (cP).sup.b Index__________________________________________________________________________1 H n-octyl 100% -- -- -- 2.18 6.49 1582 H n-decyl 100% -- -- -- 3.03 10.37 1613 H n-dodecyl 100% -- -- -- 4.13 15.64 1784 H n-octyl -- 100% -- -- 3.68 15.58 -- 1676 1245 H n-decyl -- 100% -- -- 5.15 23.99 1516 Me n-decyl -- 100% -- -- 5.82 29.64 247 6,886 1437 H/Me = n-decyl -- 100% -- -- 5.60 27.82 242 5,800 145 1/18 H n-dodecyl -- 100% -- -- 6.99 35.26 1509 H n-octyl -- -- 100% -- 5.99 33.43 363 15,386 12510 H n-decyl -- -- 100% -- 7.99 46.70 602 14,958 14311 H isodecyl -- -- X -- 11.68 119.60 2,584 556,000 8312 H isotridecyl -- -- X -- 20.09 310.22 12,700 solid 7113 H 2-octyldodecyl 15% 85% -- -- 15.10 114.97 1,500 224,000 13614 H 2-decyltetradecyl 40% 60% -- -- 16.34 118.51 14815 H n-dodecyl -- -- 50% 50% 11.91 83.19 153__________________________________________________________________________ .sup.a ASTM D445 .sup.b ASTM D3829 .sup.c ASTM D2270
TABLE 10__________________________________________________________________________Low Temperature Properties of Representative Alkylcyclopentanes ##STR22## X = MRV.sup.a, cp CCS .sup.b, cp Pour.sup.cSample # R.sub.1 R.sub.2 2 3 4 5 -30.degree. C. -25.degree. C. Point, .degree.F.__________________________________________________________________________1 H n-octyl 100% -- -- -- -102 H n-decyl 100% -- -- -- +403 H n-dodecyl 100% -- -- -- +704 H n-octyl -- 100% -- -- 720 <500 .sup. <-70.degree.5 H n-decyl -- 100% -- -- -206 H n-dodecyl -- 100% -- -- +157 H n-octyl -- -- 100% -- 3,662 1,640 <-558 H n-decyl -- -- 100% -- 4,498 2,385 <-759 H n-dodecyl -- 40% 60% -- +510 H n-decyl -- 20% 70% 10% 3,375 2,263 <-6511 Me n-octyl -- 40% 60% -- 2,171 1,200 .sup. <-60.degree.12 Me n-decyl -- 67% 33% -- 2,549 1,850 .sup. <-50.degree.13 H n-decyl -- -- 67% 33% 5,743 3,500 .sup. <-50.degree.14 Me n-decyl -- 100% -- -- 2,931 1,350 .sup. <-60.degree.15 H/Me = n-decyl -- 100% -- -- 2,681 1,188 .sup. <-50.degree. 1:116 H 2-ethylhexyl -- 95% 5% -- <-5517 H 2-octyl 15% 85% -- -- <-6518 H isodecyl -- -- X -- 103,000 >15,000 -3019 H isotridecyl -- -- X -- 369,000 solid -1520 H 2-octyldodecyl 15% 85% -- -- 20,500 11,700 60__________________________________________________________________________ .sup.a MRV = Borderline pumping test by minirotary viscometer (ASTM D38 29) .sup.b CCS = Cold cranking simulator (ASTM D2062) .sup.c Pour Point (ASTM D97)
TABLE 11__________________________________________________________________________High Temperature Properties of Alkylcyclopentanes ##STR23## Flash.sup.a Fire.sup.b X = Point, Point, Evaporation.sup.cSample # R.sub.1 R.sub.2 2 3 4 5 .degree.F. .degree.F. Loss, %__________________________________________________________________________1 H n-decyl -- 100% -- -- 500 565 0.52 H n-decyl -- 45% 50% 5% 520 580 --3 H n-decyl -- -- 67% 33% 550 620 --4 H n-dodecyl -- 40 60% -- 560 625 0.1__________________________________________________________________________ .sup.a ASTM D92 .sup.b ASTM D92 .sup.c ASTM D972, 400.degree. F., 6.5 hr., 2L/min N.sub.2
EXAMPLE 11
To evaluate the hydrocarbon substituted cyclopentadienes for lubricating properties, tests were carried out to measure physical properties which are relevant to use as a synthetic lubricant. Set forth in the following Table 12 are viscosity and pour point properties of the indicated alkyl substituted cyclopentadienes. In the cyclopentadienes tested, R.sub.1 is hydrogen, x is 2 to 6 and R.sub.2 is as indicated.
TABLE 12______________________________________Viscometric Properties of Alkylcyclopentadienes Vis Vis Vis- Pour.sup.c (100.degree. C.) (40.degree. C.) cosity.sup.b Point,Sample R.sub.2 .dbd. cSt.sup.a cSt.sup.a Index .degree.F.______________________________________1 n-Butyl 2.65 12.69 -3 <-602 n-Decyl 5.00 22.35 157 03 n-octyl/n-decyl 6.06 31.04 146 -54 2-octyl-1-dodecyl 12.78 93.38 133 -50______________________________________ .sup.a - ASTM D445 .sup.b - ASTM D2270 .sup.c - ASTM D97
The invention has been described herein with reference to certain preferred embodiments. However, as obvious variations thereon will become apparent to those skilled in the art, the invention is not to be considered as limited thereto.

Number	Name	Date
2088598	Ipatieff et al.	Aug 1937
2953607	Hafner	Sep 1960
3004384	Saunders	Oct 1961
3131227	Vries	Apr 1964
3214483	Cripps	Oct 1965
3251897	Wise	May 1966
3255267	Fritz	Jun 1966
3356704	Marcus	Dec 1967
3358008	Marcus	Dec 1967
3388180	Marcus	Jun 1968
3391209	Marcus	Jul 1968
3403105	Sandri	Sep 1962
3414626	Marcus	Dec 1968
3419622	Marcus	Dec 1968
3560583	Stewart	Feb 1971
3636176	Hall	Jan 1972
3751500	Hall	Aug 1973
3755492	Anderson	Aug 1973
3931334	Gemmill, Jr.	Jan 1976
4063010	Marie et al.	Dec 1977
4147640	Jayne et al.	Apr 1979
4246373	Kennedy et al.	Jan 1981
4412088	Gruber et al.	Oct 1983
4547603	Rajan	Oct 1985
4567308	Yoshida et al.	Jan 1986
4604492	Shimizu et al.	Aug 1986

Number	Date	Country
55535	Sep 1968	PLX
55571	Sep 1968	PLX

Lubricants comprising novel cyclopentanes, cyclopentadienes, cyclopentenes, and mixtures thereof and methods of manufacture

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Entry
Denis, J., Synthetic Lubrication, 1, 201, (1985).
Hirsch, Thesis, University of Maryland, (1963).