CA1248543A - Preparation of gossyplure - Google Patents
Preparation of gossyplureInfo
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- CA1248543A CA1248543A CA000551147A CA551147A CA1248543A CA 1248543 A CA1248543 A CA 1248543A CA 000551147 A CA000551147 A CA 000551147A CA 551147 A CA551147 A CA 551147A CA 1248543 A CA1248543 A CA 1248543A
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Abstract
Abstract of the Disclosure Process for the production of the insect sex attractant, gossyplure, is provided. The process comprises first disproportionating 1,5-cyclooctadiene and 1-hexene to give 1,5,9-tetradecatriene, then metallating the triene to form a 1-metallo-5,9-tetradecadiene, and finally treating the organometal compound with a C2-synthon to give directly 7,11-hexadecadienyl acetate or a substituted 7,11-hexadecadienyl moiety which can readily be converted to the desired acetate.
Description
PATENT
31722C~1 ~Z485~3 PREPARATION OF GOSSYPLIRE
Background This invention relates to the preparation of gossyplure.
Gossyplure, a mixture of 7,11-hexadecadienyl acetate stereoisomers, is a known pheromone for several insect species. In order to make this compound widely available for use in insect control, economic large scale synthetic conversion processes must be developed.
While synthetic routes for the preparation of gossyplure have been disclosed in the prior art, the known routes suffer from the disadvantages of requiring multiple reaction steps with consequent low over all product yield, consumption of large quantities of reagents which do not contribute to the final product structure and the like.
For example, in W.S. 3,919,329 (1975), Anderson and Henrick disclose a multistep synthesis which involves (1) the oxidation of 1,5-cyclooctadiene to 1,2-epoxy 5-cyclooctene, (2) oxidation of the epoxide to 2-hydroxy-5-cycloocten-1-one, (3) oxidative cleavage of the ~-hydroxyketone to an alkyl-8-oxo-4-octenoate, (4) Wittig reaction of the octenoate to yield (4Z, 8Z/E)-4,8-tridecadienoate, (5~ reduction of the dienoate to a dienol, (6) conversion of the dienol to the mesylate, which is then (7) converted to the iodide or bromide, which is finally (8) coupled with a cuprate reagent prepared from cuprous iodide and the lithium reagent obtained from the reaction of lithium and the bromo-acetal obtained from 3-bromo-1-propanol and ethyl vinyl ether. The product acetal is (9) hydrolyzed to 7,11-hexadecadienol, and finally (10) converted into the acetate using acetic anhydride in pyridine.
~ i~,485~3 ~ 31722CAl In U.S. 3,996,270 (1976), Friedman and Chanan describe an alternative multistep synthesis of gossyplure which involves (1) butylation of the mono-anion of 1,5-hexadiyne, (2) partial reduction of the resulting l,5-decadiyne in sodium!liquid ammonia to yield deca-(E)-5-enyne, (3) alkylation of the enyne with hexamethylene halohydrin or a protected derivative thereof, (4) acetylation of the product of step (3), which product is then (5) partially reduced in the presence of hydrogen and Lindlar catalyst. This synthesis requires several starting chemicals which are not readily available on large scale, e.g. 1,5-hexadiyne and hexamethylene halohydrin, and depend Eor the desired product stereochemistry on two separate hydrogenation steps.
Yet another multistep synthetic route for the preparation of gossyplure has been proposed by Muchowski and Venuti, as disclosed in U.S. 4,296,~42 (1981). Thus, (1) an omega-hydroxyalkyl diphenyl phosphine is converted into a cyclic polymethylene 1,1-diphenyl phosphonium bromide, (2) the cyclic phosphonium bromide is then converted into a cyclic phosphonium ylid by treatment with an alkali metal alkoxide, then (3) coupled with a protected aldehyde or ketone to produce a phosphine oxide. The phosphine oxide is (4) treated with an organolithium compound, then (5) coupled with a second aldehyde and finally (6) the resulting lithium salt is decomposed, producing a crude, protected dien-ol. The protected dien-ol is (7) hydrolyzed and esterified by treatment with acetic acid/acetyl chloride. Again, numerous reaction steps are required as the desired chain length and stereochemistry are achieved in a piecemeal fashion.
In summary, due to the large number of reaction steps required, the relative inavailability of many needed reagents and the step-wise fashion in which the desired carbon backbone is constructed, known synthetic routes for the production of gossyplure are not amenable to being carried out economically on a large scale.
Objects of the Invention An object of the invention, therefore, is an efficient and economic process for the synthesis of gossyplure.
This and other objects will become apparent from further study of the disclosure and claims herein provided.
~2~5~3 . 31722CA1 Statement of the Invention In accordance with the present invention, we have discovered that disproportionation of l,5-cyclooctadiene and l-hexene in the presence of a disproportionation catalyst produces 1,5,9-tetrade~atriene having a high selectivity to cis double bond at C-5 and greater than a thermodynamic ratio of cis/trans double bond at C-9, i.e., the desired stereochemistry at both double bonds for ultimate use as an insect sex attractant. Metallation of the resulting 1,5,9-tetradecatriene produces l-metallo-5,9-tetradecadiene which can then be reacted with a C2-synthon to give gossyplure directly or a functionally substituted C16 compound which can conveniently be converted to gossyplure.
Detailed Description of the Invention In accordance with the present invention, a process for the preparation of gossyplure is provided comprising:
(a) disproportionating 1,5-cyclooctadiene and l-hexene in the presence of a disproportionation catalyst under disproportionation conditions suitable to give 1,5,9-tetradecatriene, (b) metallating the resulting 1,5,9-tetradecatriene with a metallating agent under suitable conditions to give a 1-metallo-5,9-tetradecadiene, (c) contacting the l-metallo-5,9-tetradecadiene obtained from step (b) with a C2-synthon which is reactive with the metallo-substituted diene to give gossyplure directly or a l-substituted-7,11-hexadecadiene wherein the 1-substituent can readily be converted to the acetate, thereby giving gossyplure.
The disproportionation of 1,5-cyclooctadiene and l-hexene can be carried out in a variety of ways as recognized by those of skill in the art. Thus, any suitable ratio of 1,5-cyclooctadiene/1-hexene can be employed in the presence of a wide variety of disproportionation catalysts. For most efficient utilization of the olefinic reactants, a molar ratio of about 1:1 is preferred, although good conversions are obtained with 1,5-cyclooctadiene/1-hexene ratios ranging from about 5:1 to about 1:5.
A wide variety of heterogeneous and homogeneous disproportionation catalysts are known in the ar~ and are capable of promoting the disproportionation of l,5-cyclooctadiene plus l-hexene to ~ 4 lZ48~43 31722CAI
produce 1,5,9-tetradecatriene. Our invention is not limited to the use of a specific disproportionation catalyst, but any catalyst suitable for disproportionation of 1,5-cyclooctadiene and l-hexene can be utilized.
Suitable heterogeneous catalysts useful in the practice of the present invention include:
(1) silica or thoria promoted by an oxide or compound convertible to an oxide by calcination, or sulfide of tungsten or molybdenum; or by an oxide or compound convertible to an oxide by calcination of rhenium or tellurium;
31722C~1 ~Z485~3 PREPARATION OF GOSSYPLIRE
Background This invention relates to the preparation of gossyplure.
Gossyplure, a mixture of 7,11-hexadecadienyl acetate stereoisomers, is a known pheromone for several insect species. In order to make this compound widely available for use in insect control, economic large scale synthetic conversion processes must be developed.
While synthetic routes for the preparation of gossyplure have been disclosed in the prior art, the known routes suffer from the disadvantages of requiring multiple reaction steps with consequent low over all product yield, consumption of large quantities of reagents which do not contribute to the final product structure and the like.
For example, in W.S. 3,919,329 (1975), Anderson and Henrick disclose a multistep synthesis which involves (1) the oxidation of 1,5-cyclooctadiene to 1,2-epoxy 5-cyclooctene, (2) oxidation of the epoxide to 2-hydroxy-5-cycloocten-1-one, (3) oxidative cleavage of the ~-hydroxyketone to an alkyl-8-oxo-4-octenoate, (4) Wittig reaction of the octenoate to yield (4Z, 8Z/E)-4,8-tridecadienoate, (5~ reduction of the dienoate to a dienol, (6) conversion of the dienol to the mesylate, which is then (7) converted to the iodide or bromide, which is finally (8) coupled with a cuprate reagent prepared from cuprous iodide and the lithium reagent obtained from the reaction of lithium and the bromo-acetal obtained from 3-bromo-1-propanol and ethyl vinyl ether. The product acetal is (9) hydrolyzed to 7,11-hexadecadienol, and finally (10) converted into the acetate using acetic anhydride in pyridine.
~ i~,485~3 ~ 31722CAl In U.S. 3,996,270 (1976), Friedman and Chanan describe an alternative multistep synthesis of gossyplure which involves (1) butylation of the mono-anion of 1,5-hexadiyne, (2) partial reduction of the resulting l,5-decadiyne in sodium!liquid ammonia to yield deca-(E)-5-enyne, (3) alkylation of the enyne with hexamethylene halohydrin or a protected derivative thereof, (4) acetylation of the product of step (3), which product is then (5) partially reduced in the presence of hydrogen and Lindlar catalyst. This synthesis requires several starting chemicals which are not readily available on large scale, e.g. 1,5-hexadiyne and hexamethylene halohydrin, and depend Eor the desired product stereochemistry on two separate hydrogenation steps.
Yet another multistep synthetic route for the preparation of gossyplure has been proposed by Muchowski and Venuti, as disclosed in U.S. 4,296,~42 (1981). Thus, (1) an omega-hydroxyalkyl diphenyl phosphine is converted into a cyclic polymethylene 1,1-diphenyl phosphonium bromide, (2) the cyclic phosphonium bromide is then converted into a cyclic phosphonium ylid by treatment with an alkali metal alkoxide, then (3) coupled with a protected aldehyde or ketone to produce a phosphine oxide. The phosphine oxide is (4) treated with an organolithium compound, then (5) coupled with a second aldehyde and finally (6) the resulting lithium salt is decomposed, producing a crude, protected dien-ol. The protected dien-ol is (7) hydrolyzed and esterified by treatment with acetic acid/acetyl chloride. Again, numerous reaction steps are required as the desired chain length and stereochemistry are achieved in a piecemeal fashion.
In summary, due to the large number of reaction steps required, the relative inavailability of many needed reagents and the step-wise fashion in which the desired carbon backbone is constructed, known synthetic routes for the production of gossyplure are not amenable to being carried out economically on a large scale.
Objects of the Invention An object of the invention, therefore, is an efficient and economic process for the synthesis of gossyplure.
This and other objects will become apparent from further study of the disclosure and claims herein provided.
~2~5~3 . 31722CA1 Statement of the Invention In accordance with the present invention, we have discovered that disproportionation of l,5-cyclooctadiene and l-hexene in the presence of a disproportionation catalyst produces 1,5,9-tetrade~atriene having a high selectivity to cis double bond at C-5 and greater than a thermodynamic ratio of cis/trans double bond at C-9, i.e., the desired stereochemistry at both double bonds for ultimate use as an insect sex attractant. Metallation of the resulting 1,5,9-tetradecatriene produces l-metallo-5,9-tetradecadiene which can then be reacted with a C2-synthon to give gossyplure directly or a functionally substituted C16 compound which can conveniently be converted to gossyplure.
Detailed Description of the Invention In accordance with the present invention, a process for the preparation of gossyplure is provided comprising:
(a) disproportionating 1,5-cyclooctadiene and l-hexene in the presence of a disproportionation catalyst under disproportionation conditions suitable to give 1,5,9-tetradecatriene, (b) metallating the resulting 1,5,9-tetradecatriene with a metallating agent under suitable conditions to give a 1-metallo-5,9-tetradecadiene, (c) contacting the l-metallo-5,9-tetradecadiene obtained from step (b) with a C2-synthon which is reactive with the metallo-substituted diene to give gossyplure directly or a l-substituted-7,11-hexadecadiene wherein the 1-substituent can readily be converted to the acetate, thereby giving gossyplure.
The disproportionation of 1,5-cyclooctadiene and l-hexene can be carried out in a variety of ways as recognized by those of skill in the art. Thus, any suitable ratio of 1,5-cyclooctadiene/1-hexene can be employed in the presence of a wide variety of disproportionation catalysts. For most efficient utilization of the olefinic reactants, a molar ratio of about 1:1 is preferred, although good conversions are obtained with 1,5-cyclooctadiene/1-hexene ratios ranging from about 5:1 to about 1:5.
A wide variety of heterogeneous and homogeneous disproportionation catalysts are known in the ar~ and are capable of promoting the disproportionation of l,5-cyclooctadiene plus l-hexene to ~ 4 lZ48~43 31722CAI
produce 1,5,9-tetradecatriene. Our invention is not limited to the use of a specific disproportionation catalyst, but any catalyst suitable for disproportionation of 1,5-cyclooctadiene and l-hexene can be utilized.
Suitable heterogeneous catalysts useful in the practice of the present invention include:
(1) silica or thoria promoted by an oxide or compound convertible to an oxide by calcination, or sulfide of tungsten or molybdenum; or by an oxide or compound convertible to an oxide by calcination of rhenium or tellurium;
(2) alumina promoted with an oxide or compound convertible to an oxide by calcination of molybdenum, tungsten, or rhenium; a sulfide of tungsten or molybdenum; or an alkali metal salt, ammoniurn salt, alkaline earth metal salt, or bismuth salt of phosphomolybdic acid;
(3) one or more of the group aluminum phosphate, zirconium phosphate, calcium phosphate, magnesium phosphate, or titanium phosphate promoted by one or more of a sulfide of molybdenum or tungsten, or an oxide or compound convertible to an oxide by calcination of molybdenum, tungsten or rhenium or magnesium tungstate or beryllium phosphotungstate;
(4) silica, alumina, aluminum phosphate, zirconium phosphate, calcium phosphate, magnesium phosphate, or titanium phosphate promoted by a hexacarbonyl of molybdenum or tungsten; and
(5) (a) molybdenum oxide or tungsten oxide associated with suitable support material and (b) at least one organoaluminum compound, optionally, treated with nitric oxide or nitrosyl halides.
The catalysts of (1) can be prepared and activated by conventional techniques such as by combining a catalyst grade silica with suitable tungsten, molybdenum, rhenium or tellurium compounds by a conventional method such as, for example, impregnation, dry mixing, or co-precipitation. Suitable tungsten and molybdenum compounds include tungsten oxide and molybdenum oxide and compounds convertible to these oxides. The supported oxides are activated by calcining in air and the supported sulfides are activated by heating in an inert atmosphere.
The catalysts of (2) can be prepared and activated by conventional techniques such as by combining catalyst grade alumina with an oxide or a compound convertible to an oxide by calcination of molybdenum, tungsten or rhenium and calcining the resulting mixture after ~248543 31722CAl removal of any solvent used in the impregnation. The sulfides of tungsten or molybdenum or the salts of phosphomolybdic acid can be utilized to impregnate a catalyst grade alumina by solution in a proper solvent after which the solvent is evaporated and the resulting mixture dried to prepare the catalyst.
The catalyst compositions of (3) can be prepared and activated by conventional techniques. For example, molybdenum oxide can be co-precipitated with aluminum phosphate followed by calcination in air to produce an activated catalyst. Alternatively, the support material can be impregnated with a compound of the promoter convertible to the oxide, such as ammonium tungstate, followed by calcination in air. In the preparation of a sulfide-containing catalyst, a sulfide of the promoter can be ball-milled with a support, such as zirconium phosphate, followed by heating in an inert atmosphere such as nitrogen. Magnesium tungstate and beryllium phosphotungstate can be dry mixed with titanium phosphate, for example, and activated by calcination in air at elevated temperatures.
The catalyst compositions of (4) can be prepared and activated by impregnating a previously calcined support material such as calcium phosphate with a solution of the hexacarbonyl of the promoter in an organic solvent such as benzene, followed by drying in a vacuum or in an inert atmosphere at about 50 to 700F.
The (a) components of the catalyst system (5) are active by themselves for the disproportionation of olefins. However, the activity of this system is exhibited at relatively high temperatures which are generally above 150C for optimum operation.
Suitable support materials which are combined with the oxides of molybdenum and tungsten to form the (a) component of the catalyst system (5) include alumina, silica, silica-alumina magnesia-titania, thoria, aluminum phosphate, zirconium phosphate, titanium phosphate, calcium phosphate, magnesium phosphate, and mixtures thereof.
Preferred combinations of the above support materials with the oxides of molybdenum and tungsten promoter materials include (i) silica or thoria promoted by the oxide or a compound convertible to an oxide by calcination of tungsten or molybdenum; (ii) alumina promoted by an oxide, or compound convertible to an oxide by calcination of molybdenum or ~ 1~485~3 31722CAl tungsten; and (iii) one or more of the group aluminum phosphate, zirconiu~ phosphate, calcium phosphate, magnesium phosphate, or titanium phosphate promoted by one or more of an oxide of molybdenum or tungsten, or by a compound of molybdenum or tungsten convertible to an o~ide by calcination.
The combinations of (i), (ii), or ~iii) can be prepared and activated by suitable methods such as, ~or example, impregnation, dry mixing, or co-precipitation.
When the promoter is tungsten oxide, the preferred support material is silica or silica-containing materials. The preferred support material for molybdenum oxide is alumina or alumina-containing materials.
In general the (a) component of the catalyst system (5) will contain about 0.1 to about 30, preferably from about 1 to about 15 weight percent of the molybdenum or tungsten oxide. In addition, it is sometimes desirable that this component of the catalyst system of the invention contain relatively small amounts, from about 0.005 to about 5, preferably 0.1 to 2, weight percent of an inorganic base material. Suitable inorganic base materials include alkali metal and alkaline earth metal hydroxides and carbonates, sodium hydroxide, potassium hydroxide, sodium carbonate and potassium carbonate being preferred.
The solid (a) component of the system (5) catalysts can be in any conventional catalytic shape or size, depending upon the type of conversion in which it is to be utilized. For example, in fixed bed catalyst syste~s, the solid composite can be in the form of spheres, pellets, extrudates, agglomerates and the like. In slurry catalyst systems, the solid can be in the form of relatively small particles or in the form of a powder.
To be effective in the present catalyst system, the above-described (a) component of the catalyst system t5) is activated at elevated temperatures, generally in flowing air. The activation of the catalysts is accomplished at a temperature ranging from about 500 to 1600F for a period of several seconds to several hours. When the (a) component of the catalyst system is tungsten oxide on silica, a convenient and economical activation treatment is in the temperature range of about 900 to 1200F for a period of 15 minutes to 5 hours.
When the (a) component of the catalyst system (5) is molybdenum oxide on 7 ~Z^~S~3 31722CAI
alumina, a convenient and economical treatment is in the temperature range of about 900-1400F for 0.5 to 20 hours or longer. In some cases the activation using an oxygen-containing gas can be followed by treatment, also at elevated temperatures, with other treating gases such as carbon monoxide, hydrogen and the like.
The organoaluminum compounds which are applicable for use as the (b) component in catalyst (5) have the formula R"aAlXb where R" is a saturated aliphatic or aromatic hydrocarbon having up to about 20 carbon atoms. X is chlorine, bromine, iodine, or fluorine, a is an integer of at least 1, b can be 0, 1 or 2, and the total of a and b is 3, thus a can be 1, 2 or 3. Such aluminum compounds are well known in the art and are generally commercially available.
Some examples of suitable organoaluminum compounds halide are methylaluminum dichloride, dimethylaluminum fluoride, methylaluminum sesquichloride, trimethylaluminum, ethylaluminum dichloride, ethylaluminum sesquichloride, di(2-ethylhexyl)aluminum bromide, triisobutylaluminum, phenylaluminum dichloride, di(3 methylpentyl)aluminum bromide, cyclohexylaluminum dichloride, benzylaluminum diodide, dieicosylaluminum bromide, and the like, and mixtures thereof. The preferred (b) components are the organoaluminum halides, especially those wherein the hydrocarbon portion is an alkyl radical of 1 to 5 carbon atoms. Particularly good results are obtained with ethylaluminum dichloride, diethylaluminum chloride, and mixtures such as ethylaluminum sesquichloride and methylaluminum sesquichloride.
The molar proportion of the organoaluminum (b) component to the solid (a) component to form the catalyst system (5) useful in the practice of the present invention will generally be in the range of from about 0.005:1 to 20:1, preferably from about 0.01:1 to 10:1 moles of the (b) component per mole of the molybdenum or tungsten oxide contained in the (a) component.
It is sometimes preferred that the supported tungsten or molybdenum component, before contacting the organoaluminum compound, be treated either with nitric oxide or with a nitrosyl halide. Such treatment can take place at a temperature preferably in the range of about 0 to 130C, more preferably about 20 to 60C, for a time in the range of from a few seconds up to about 24 hours, and preferably in the ~ 317220A1 8 ~:~48543 presence of a diluent in which the nitric oxide or nitrosyl halide is at least partially soluble. After such treatment, the diluent and excess nitric oxide or nitrosyl halide can be removed from the solid catalyst by decantation, evaporation, and similar techniques. This treatment, however, should be carried out in the substantial absence of moisture, preferably in an inert atmosphere, to preserve the effects of the previous activation by calcination.
The catalyst system (5) useful in the practice of the present invention is prepared simply by combining the solid (a) component with the organoaluminum (b) component under conditions of time and temperature which permit the catalytically active catalyst composition to be formed.
The combination occurs very readily, and, in general, the components can be mixed at any convenient temperature, room temperature frequently being satisfactory, in the presence of a diluent in which the organoaluminum compound is at least partially soluble. Any convenient diluent such as, for example, benzene, cyclohexane, toluene, chiorobenzene, methylene chloride, ethylene chloride, and the like, can be used for this purpose.
Halogenated diluents are generally preferred. The mixing of these two catalyst components is carried out in the substantial absence of air or moisture, generally in an inert atmosphere. After the catalytic reaction mixture is formed, it need not be isolated but can be added directly to the olefin reaction zone as a suspension in its preparation medium. If desired, the catalyst components can be separately added, in any order, to the reaction zone either in the presence or absence of the feed olefin.
Alternatively, the system (5) catalysts useful in the practice of the invention can be separated from the preparation medium and the dissolved organoaluminum compound therein by decantation, and, after additional washing and/or drying if desired, can be added to the reaction zone as a solid rather than as a suspension.
The operating temperature for the process of this invention when using heterogeneous catalysts of (1) is in the range of about 400 to 1100F. The process of this invention when using the catalysts of (2) will be operated at a temperature in the range of about 150 to 500F.
The process using the catalysts of (3) will be carried out in a temperature range of about 600 to 1200F. The process using the 9 ~2485~3 31722CA1 catalysts of (4) will be carried out in a temperature range of about O to 600F. In the process of the invention, pressures are not important but will be generally in the range of about 0 to 2,000 psig.
According to the process of the invention employing catalyst system (5), the mixture of olefins to be converted, i.e., 1,5-cyclooctadiene and 1-hexene, is contacted with the catalyst under conditions suitable to obtain the desired reaction, for example, at a temperature in the range of about 0 to 150C and at any convenient pressure. Preferably, the temperature is in the range of about 15C to 50C wherein good results are obtained economically. Excellent results are obtained by contacting the olefin feed material with the catalyst at room temperature. The conversion can be carried out in the presence of any inert diluent such as that used for the catalyst preparation, if desired. Diluents are not essential but are sometimes preferred and such diluents can include saturated aliphatics and aromatics such as cyclohexane, xylene, isooctane, and the like, and halogenated derivatives thereof. The time of contact will depend upon the desired degree of conversion and the catalysts utilized, but will, generally, be in the range of from 0.1 minute to 24 hours, preferably 5-120 minutes. The proportion of catalyst composition to olefin feed in the reaction zone will generally be in the range of from about 0.001 to 100 millimoles of the molybdenum or tungsten oxide contained in the solid catalyst, for each mole of olefin in the reacting zone.
The oxide-promoted catalysts useful in the practice of this invention are activated by heat treatment at temperatures of from 600 to 1500F for a period of about 1 second to 25 hours or more, shorter times being used with higher temperatures and longer times with the lower temperatures. A convenient and economical treatment is obtained by subjecting the catalyst to contact with a stream of air at a temperature in the range of about 900 to 1200F for from about 15 minutes to 5 hours.
Other gases, which do not poison the catalyst, for example, nitrogen, can also be sometimes used either as a substitute for the air treatment, or as a subsequent flush. Air is usually preferred for activation, since it is readily available.
Any conventional contacting technique can be used for the olefin disproportionation employing the heterogeneous catalysts disclosed ~ 543 31722CA1 hexein, and batchwise or continuous operation can be utilized. After the reaction period, the products can be separated and/or isolated by any suitable means such as by fractionation, crystallization, adsorption, and the like. Unconverted feed materials or products not in the desired molecular weight range can be recycled to the conversion ~one. After separation of the products, the solid catalyst can be recycled to the reaction zone either with or without the addition of a fortifying amount of organoaluminum halide.
The heterogeneous catalysts employed in the practice of the invention can be further treated with modifying amounts of compounds of alkali metals or alkaline earth metals.
The catalyst supports and promoting agents employed can contain other materials which do not have a deleterious effect on the desired reaction or promote the formation of undesired by-products.
Suitable homogeneous catalysts employed in the practice of the present invention include:
(a) the coordination compounds of molybdenum or tungsten as disclosed in U.S. 3,778,385;
(b) the coordination compounds of molybdenum or tungsten complexed with N0, together with an organoaluminum adjuvant, as disclosed in U.S. 4,010,217;
(c) the neutral carbene complex catalysts disclosed in U.S. 4,247,417;
(d) the neutral carbene complex catalysts disclosed in ~.S. 4,248,738;
(e) the neutral carbene complex catalysts disclosed in U.S. 4,269,780;
(f) other homogeneous catalysts known by those of skill in the art such as, for example, WCl6+SnMe~; W(CH2C6H5)3Cl+AlCl3; WOCl4+R4Sn;
and the like.
It is also recognized by those of skill in the art that the homogeneous catalysts detailed herein can be deposited on solid support and employed as solid phase catalysts.
The metallation of 1,5,9-tetradecatriene to form 1-metallo-5,9-tetradecadiene can be carried out employing a variety of 11 ~Z48543 31722CAl metallating agents. Any metallating agent capable of selective reaction with the terminal double bond of the triene starting material is suitable. Examples of suitable metallating agents include organoboranPs, organoaluminum compounds, organomagnesium compounds, organozirconium compounds and the like.
Organoboranes contemplated to be within the scope of the present invention can be described as "hindered" organoborane compounds and can be represented by the following formula:
wherein each R is independently a Cl to C10 carbon radical wherein at least one R group is a secondary or tertiary alkyl group and each R group can be connected to the other as part of a ring structure. Exemplary compounds which satisfy the above formula include disiamylborane (i.e., bis-(3-methyl-2-butyl)borane), 9-borabicyclo [3.3.1] nonane (9-BBN), dithexylborane, thexylcyclopentylborane, thexylcyclohexylborane, and the like.
The hydroboration reaction is generally carried out in the presence of a suitable solvent such as, for example, tetrahydrofuran (THF). A roughly equimolar mixture of triene and organoborane reagent are combined. Preferably, a slight excess of triene is employed to minimize the likelihood of hydroboration occurring on the internal double bonds of the starting material triene. Typically, the hydroboration reaction should be carried out in an inert atmosphere; i.e. moisture and oxygen should be excluded from the reaction mixture. Reaction conditions employed are broadly 0-100C for a few minutes up to several hours.
Preferably, the hydroboration is carried out at about 20-80C for 15 minutes up to about 2 hours. Reaction is generally carried out at about atmospheric pressure, although higher and lower pressures are acceptable.
Once the reaction of the triene and organoboron compound is complete, the resulting 1-metallo-5,9-tetradecadiene is ready for further reaction with an appropriate C2-synthon as detailed more fully below.
Organoaluminum compounds contemplated to be within the scope of the present invention can be described by reference to the formula:
-lZ~543 31722CA1 R2AlH
wherein R is as defined above. Examples of suitable organoaluminum compounds include diisobutylaluminum hydride, diisopropylaluminum hydride and the like.
Organozirconium compounds contemplated to be within the scope of the present invention can be described by the formula:
(Ar)2Zr(X)H
wherein Ar is an aromatic ligand having 5-10 carbon atoms, such as phenyl, cyclopentadienyl, methylcyclopentadienyl, and the like, and X is a halogen. Examples of suitable organozirconium compounds include biscyclopentadienylzirconium chlorohydride, biscyclopentadienyl bromohydride, bispentamethylcyclopentadienyl chlorohydride, bismethylcyclopentadienyl chlorohydride, bisdimethylcyclopentadienyl chlorohydride, and the like.
Organomagnesium compounds contemplated to be within the scope of the present invention can be described by reference to the following formulae:
R'MgX, and R'2Mg wherein R' has at least one ~-hydrogen, and therefore is a C2 to C1O
carbon radical and X is Cl, Br or I. Exemplary compounds which satisfy the above formulae include various Grignard reagents, such as, for example, ethylmagnesium bromide, isopropylmagnesium bromide, butyl-magnesium bromide, and the like. Additional examples include dialkyl-magnesium compounds such as, for example, diethylmagnesium, diisopropyl-magnesium and the like.
Metallation with organomagnesium compounds is generally carried out in the presence of at least one transition metal activating agent.
Suitable transition metal activating agents include nickel, titanium, vanadium and zirconium compounds. Exemplary titanium activating agents include a titanocene dichloride such as, for example, dicyclopentadiene 13 1 2 g 8 5 4 3 31722CAl titanium dichloride, or alternatively, titanium tetrachloride. The molar ratio of organomagnesium compound to triene should be at least about 1:1 with the presence of a small excess of the organomagnesium compound acceptable, i.e., up to about to a 1.5 to 1 molar ratio. The molar ratio of triene to transition metal reagent is generally in the range of about 1-500:1 and preferably about 50-100:1.
Metallation with organomagnesium compounds is generally carried out at atmospheric pressure, although higher and lower pressures are operable. Preferably, atmospheric pressure or slightly reduced pressures will be employed since pressures in excess of atmospheric will tend to retard the reaction rate. Reaction temperatures of about -20 to about 100C for at least one minute up to about 24 hours are suitable.
Preferably, reaction temperature will be maintairled between about 0 and 60~C, for about 15 minutes to about 6 hours.
Conversion of the 1-metallo-5,9-tetradecadiene to a 1-substituted-7,11-hexadecadiene can be carried out by contacting the metallo-diene with a variety of C2-synthons which are reactive with the organometallic species. Exemplary reactive C2-synthons include ethylene oxide, bromoethyl acetate (BrCH2CH20COCH3), ethyl bromoacetate (BrCH2C02Et), diethyl bromomalonate, chloroethyl acetate, ethyl chloroacetate, iodoethyl acetate, ethyl iodoacetate and the like. The product is a substituted hexadecadiene or derivative thereof, which has the empirical formula, C15H27Z, wherein Z is selected from the group consisting of -CH20H, -C02CH3, and -CH20COCH3.
The 1-metallo-5,g-tetradecadiene can be contacted with an appropriate C2-synthon under suitable reaction conditions to cause the formation of a new carbon-carbon sigma bond. Thus, for example, an organoborane can be contacted with a halo-ester in the presence of a suitable base such as, for example, potassium t-butoxide. Alternatively, an organomagnesium compound can be contacted with ethylene oxide or a halo-ester, optionally in the presence of a copper (I) salt. Typical reaction conditions comprise inert atmosphere at -20 to 80C for 0.5 to 10 hours. Preferably, reaction is carried out at about -10 to +20C for 1-2 hours.
When a copper (I) salt is employed to promote the reaction of the 1-metallo-5,9-tetradecadiene and the C2 synthon, only catalytic ~Z4~S~3 31722CAl amounts are required. Thus, about 1-20 mole % copper (I) salt based on the moles of organometallic species employed are suitable. Preferably, about 2-10 mole % copper (I) salt will be used. Suitable copper (I) salts include copper (I) iodide, copper (I) bromide, copper (I) chloride and the like.
Where Z above is methoxy (-CH2OH), the product need only be esterified employing techniques well known to those of skill in the art in order to convert the hydroxy substituted hexadecadiene into gossyplure. Where Z above is acetoxy (-CO2CH3), the carbonyl function can conveniently be reduced to the alcohol by techniques known to those of skill in the art, such as, for example, reduction with lithium aluminum hydride, to give an alcohol which can then be converted to gossyplure by standard esterification techniques. Where Z is -CH20COCH3, i.e., when the C2-synthon employed is bromoethyl acetate, chloroethyl acetate or iodoethyl acetate, gossyplure is obtained directly as the product of the conversion of the l-metallo-5,9-tetradecadiene.
A further understanding of the present invention and its advantages will be provided by reference to the following examples.
Example I
Preparation of 1,5,9-Tetradecatriene a. Homogeneous catalyst Equimolar quantities of 1,5-cyclooctadiene and l-hexene were mixed in an inert atmosphere in an autoclave. The catalyst charge of about 0.0025 mole of (phenylmethoxycarbene)pentacarbonyltungsten(0) per mole of cyclooctadiene was added as a 0.1 molar solution in chlorobenzene along with approximately 0.025 mole of carbon tetrachloride as a catalyst modifier. A small amount of hexadecane (0.05-0.10 mole) was added in a precisely weighed amount as an internal standard for subsequent analysis by gas liquid chromatography (GLC).
The reaction was started and the reaction mixture was held at reaction temperature for about 2 hours after which time it was cooled, removed from the reactor and analyzed. Table I shows the results obtained from operating in the temperature range 84-92C.
iZ4~5~3 31722CA1 Table I
Preparation of 1,5,9-Tetradecatriene from 1,5-cyclooctadiene and 1-Hexene Using Homogenous (Phenylmethoxycarbene)pentacarbonyl tungsten (03 Catalyst b Selectivity Run Temp Press. CODa TDT to TDT, No. C psi Conv.,% Yield, % %
Time = 2 hrs a. COD = 1,5 Cyclooctadiene b. TDT = 1,5,9-Tetradecatriene (Phenylmethoxycarbene)pentacarbonyltungsten(O) was prepared by known literature procedures (e.g. Cardin, D. J. et al. Chem. Rev. 72 545 (1972)) b. Heterogeneous Catalyst An alumina-supported cobalt molybdate catalyst (American 20 Cyanamide HDS-20A; 78.7 wt.% Al203) was activated by heating in air at 350C for 3 hours, then under argon for about 0.5 hours, as the catalyst bed was cooled to about 130-160C for reaction. A 1:1.2 molar ratio of 1,5-cyclooctadiene:1-hexene was prepared over the above described activated catalyst at 130-160C and 4-10 weight hourly space velocity (WHSV). GLC analysis indicated about 16% conversion of cyclooctadiene feed and about 38% selectivity (or about 6% yield) to 1,5,9-tetradecatriene.
Example II
Coupling of 1,5,9-Tetradecatriene with Ethyl Bromoacetate using 9-Borabicyclononane.
1,5,9-Tetradecatriene (20 grams, 0.104 mole) in 50 mL of tetrahydrofuran was placed in a thoroughly dried 1 liter flask equipped with dropping bottle and a magnetic stirrer. An atmosphere of nitrogen was maintained in the flask. A tetrahydrofuran solution of 35 9-borabicyclononane (9-BBN) (200 mL of solution containing 0.100 mole of 9-BBN) was added slowly over about 15 minutes and the temperature was raised to reflux for 1 hour. The mixture was cooled to near 0C and 50 ~Z4859~3 mL of tertiary butyl alcohol and 17 grams of ethyl bromoacetate was added. One hundred milliliters of a 1 molar solution of potassium tertiary-butoxide and tertiary butyl alcohol was added dropwise over 0.5 hour The cloudy aqueous solution was warmed to room temperature and 33 m~ of 3 molar aqueous sodium acetate solution was added followed by 22 mL
of 30% hydrogen peroxide which was added dropwise. After stirring for an additional 30 minutes at room temperature the mixture was diluted with saturated aqueous sodium chloride and the solution was extracted with an approximately equal volume of diethyl ether. The separated ether solution was washed once with an approximately equal volume of saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate.
After filteration to remove the magnesium sulfate and simple distillation to remove the volatiles the yield was determined by GLC using a precisely weighed amount of methyl undecenoate as a standard. The results of several runs are shown in Table II.
17 lZ~8543 31722CA1 Table II
Coupling of 1,5,9-Tetradecatriene (TDT) with Ethyl Bromoacetate Using 9-Borabicyclononane (BBN) Run After TDT EHDDa 5 Run BBN Addition Conv. Yield Select No. Solvent Hrs. Temp.C % % %
4 THFb 1 reflux 64 36 56 10 6 C6C 3 reflux 92 28 30 8 C6 1 room temp. 68 27 41 9 C6/THF 1.5 50 44 17 38 THF 1 room temp. 40 8 21 15 11 C6 5.5 room temp. 51 49 95 12 C6 1 room temp. 50 45 90 14 THF 1 room temp. 48 39 81 THF 1 reflux 56 35 63 20 16 C6 5 reflux 61 44 72 a. EHDD = Ethyl Hexadecadienoate b. THF = Tetrahydrofuran c. C6 = n-Hexane It is seen that lower reaction temperatures favor higher selectivities and that longer reaction times favor higher conversions. The reasons for the inconsistencies shown such as in the extreme example in no. 10, are not known, but it is suspected that may be due to inconsistencies in excluding moisture from the potassium tertiary-butoxide solutions.
~ 8 1248543 31722CA1 Example III
Reduction of Ethylhexadecadienoate to 7,11-Hexadecadien-1-ol.
The ethylhexadecadienoate was reduced with lithium aluminum hydride (LAH) in tetrahydrofuran as follows. An oven dried 3-neck flask equipped with a magnetic stirrer, reflux condenser and an addition funnel was charged with 2 equivalents of LAH in dry tetrahydrofuran (THF). The reaction vessel and contents were maintained under a positive flow of nitrogen as 1 equivalent of ester (ethylhexadecadienoate) dissolved in an equal volume of dry THF was added dropwise to the stirred LAH suspension at a rate to maintain the THF at a gentle boil. After ester addition was complete, the reaction mixture was refluxed gently for an additional 2 hours, cooled to 0C and one equivalent of water slowly added to decompose excess LAH, followed by addition of 15% aqueous NaOH. The resulting gray gel was filtered and the organic layer washed with water, dried over adsorbent and concentrated on a rotary evaporator. Yields of about 41% of the desired 7,11-hexadecadien-1-ol were obtained.
The product alcohol was esterified without further purification.
Example IV
Acetylation of 7(Z),ll(Z,E)-Hexadecadien-1-ol Twenty-eight grams of 7,11-hexadecadien-1-ol and 50 ~L of acetic acid were reacted in 100 mL of refluxing toluene for 8 hours. The mixture was cooled, washed twice with water, once with a saturated sodium chloride solution and then dried over magnesium sulfate. The mixture was filtered, reduced in volume using a rotary evaporator and then distilled at reduced pressure through a short Vigreaux column. The gossyplure fraction boiling at 111-114C at 0.05 millimeters of mercury was collected and analyzed.
A crude yield of 54% of the gossyplure was obtained. Analysis showed that the double bond in the 11-position was about 62% trans (E) and 38% is (Z).
Example V
Coupling of 1,5,9-tetradectriene with ethylene oxide using Butylmagneium Chloride ~ 19 lZ~8~43 31722CAl 1,5,9-Tetradecatriene (lOg, 0.052 mo~; 88% purity by GLC), butylmagnesium chloride (18 mL of 2.8M in diethyl ether; 0.05 mol) and titanocene dichloride [bis(cyclopentadienyl)titanium dichloride; 0.15g, 0.6 mmol] were stirred under an inert atmosphere at room temperature.
After about three hours, the reaction mixture was cooled to about 0C and cuprous bromide (0.035 g, 0.2 mmol) and tetrahydrofuran (THF; 20 mL) were added. The reaction mixture was maintained between about 0-15C while ethylene oxide (EO; 3.2 mL, 0.063 mol~ was added slowly. Once EO
addition was complete, the reaction mixture was stirred for an additional 10 hour at 0C. Acetyl chloride (7.4 mL, 8.17 g, 0.1 mol) was then added dropwise to the reaction mixture. The reaction temperature rose to about 45C by the time acetyl chloride addition was complete. The rection mixture was stirred overnight at room temperature before workup for GLC
analysis.
Workup involved pouring the reaction mixture into an equal volume of cold water, separating and washing the organic layer with saturated sodium bicarbonate solution, drying the organic layer over MgS04, filtering and removing the solvent on a rotary evaporator. GLC
analysis indicated a 37% yield of gossyplure, based on triene starting material.
Example VI
Ten grams of 1,5(E),9(E,2)-tetradecatriene (52 mmole), 31.2 mL
of 2 molar butylmagnesium chloride (62.4 mmole) in diethyl ether and 0.65 g of titanocene dichloride (2.6 mmole) were mixed under an inert atmosphere and stirred at room temperature for two hours. The mixture was cooled to -30C and 50 mL of tetrahydrofuran was added. Cuprous bromide (2.24 g, 7.8 mmole) was added followed by ethylene oxide (63.2 mmole) which was added slowly with cooling to maintain the temperature of the reaction mixture in the range of -30 to 0C. Vigorous stirring was continued for about an hour while the temperature was held below 5C.
The product mixture was mixed first with ethyl acetate and washed with 4.5 molar HCl (about 2.5 moles HCl per mole of the starting triene), separated and then washed with a saturated aqueous sodium bicarbonate solution to remove any residual acid left in the organic layer. The yield of 7~2),11(E,Z)-hexadecadien-l-ol as determined by GLC
was 44%.
1248~43 31722C~l The 7(Z),ll(Z,E)-hexadecadien-l-ol can readily be separated by distillation. Most of the yields shown in the following tabulations were determined by GLC using a methyl silicone coated capillary column held at 80C for 2 minutes followed by temperature programmed increase of 10C/minute up to 250C.
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`S `S ~ ~J ~ `S `S ~ `S ~S ~ ~ ~ ~ ~ ~ ~ ~ D O E-l , " ~3 31722CAl The data in Table III indicate that the results are fairly consistent over more than an 80-fold increase in the scale of the reaction. Runs 1-6 show that only very small amounts of copper (I) bromide are required to produce good results in the reaction of ethylene oxide with the Grignard intermediate under the conditions used. Table IV
shows that presence of CuBr is necessary when the solvent is THF but may not be necessary in ether.
Run 40, Table V, shows that TiCl4 can be used effectively in ether solutions in place of titanocene dichloride in the transfer of MgCl0 from the butyl Grignard to the tetradecatriene moiety.
Example VII
Coupling of 1,5,9-Tetradecatriene with Bromethyl Acetate using Butylmagnesium Chloride 1,5,9-Tetradecatriene (lOg, 0.052 mol), n-butylmagnesium chloride (24.8 mL of 2.5 M in tetrahydrofuran; 0.062 mol) and titaniwn tetrachloride (0.52g, 0.0027 mol) were stirred under an inert atmosphere at about 65C for about 4.5 hours. The reaction mixture was then cooled to 0C and cuprous bromide (0.14g, 1.0 mmol) was added. 2-Bromoethyl acetate (6.9 mL, 0.063 mol) was then added dropwise and the mixture allowed to warm slowly to room temperature and stirred for several hours at room temperature. Reaction temperature was then raised to 60C for 4 hours before the mixture was cooled, acidified with aqueous HCl, then extracted with hexane. The hexane extract was washed with saturated sodium bicarbonate solution, dried over MgS04, filtered and solvent removed on the rotary evaporator. GLC analysis of this crude reaction product indicated an 11% yield of gossyplure. It should be recognized that while this reaction represents successful production of gossyplure from 1,5,9-tetradecatriene in one reaction vessel, the reaction parameters have not been optimized. Consequently, significantly improved yields of gossyplure can be expected upon optimization of various reaction parameters.
The examples have been provided merely to illustrate the practice of our invention and should not be read so as to limit the scope of our invention or the appended claims in any way. Reasonable variations and modifications, not departing from the essence and spirit ~ ~ ' 31722CAl l.Z48543 of our invention, are contemplated to be within the scope of patent protection desired and sought.
The catalysts of (1) can be prepared and activated by conventional techniques such as by combining a catalyst grade silica with suitable tungsten, molybdenum, rhenium or tellurium compounds by a conventional method such as, for example, impregnation, dry mixing, or co-precipitation. Suitable tungsten and molybdenum compounds include tungsten oxide and molybdenum oxide and compounds convertible to these oxides. The supported oxides are activated by calcining in air and the supported sulfides are activated by heating in an inert atmosphere.
The catalysts of (2) can be prepared and activated by conventional techniques such as by combining catalyst grade alumina with an oxide or a compound convertible to an oxide by calcination of molybdenum, tungsten or rhenium and calcining the resulting mixture after ~248543 31722CAl removal of any solvent used in the impregnation. The sulfides of tungsten or molybdenum or the salts of phosphomolybdic acid can be utilized to impregnate a catalyst grade alumina by solution in a proper solvent after which the solvent is evaporated and the resulting mixture dried to prepare the catalyst.
The catalyst compositions of (3) can be prepared and activated by conventional techniques. For example, molybdenum oxide can be co-precipitated with aluminum phosphate followed by calcination in air to produce an activated catalyst. Alternatively, the support material can be impregnated with a compound of the promoter convertible to the oxide, such as ammonium tungstate, followed by calcination in air. In the preparation of a sulfide-containing catalyst, a sulfide of the promoter can be ball-milled with a support, such as zirconium phosphate, followed by heating in an inert atmosphere such as nitrogen. Magnesium tungstate and beryllium phosphotungstate can be dry mixed with titanium phosphate, for example, and activated by calcination in air at elevated temperatures.
The catalyst compositions of (4) can be prepared and activated by impregnating a previously calcined support material such as calcium phosphate with a solution of the hexacarbonyl of the promoter in an organic solvent such as benzene, followed by drying in a vacuum or in an inert atmosphere at about 50 to 700F.
The (a) components of the catalyst system (5) are active by themselves for the disproportionation of olefins. However, the activity of this system is exhibited at relatively high temperatures which are generally above 150C for optimum operation.
Suitable support materials which are combined with the oxides of molybdenum and tungsten to form the (a) component of the catalyst system (5) include alumina, silica, silica-alumina magnesia-titania, thoria, aluminum phosphate, zirconium phosphate, titanium phosphate, calcium phosphate, magnesium phosphate, and mixtures thereof.
Preferred combinations of the above support materials with the oxides of molybdenum and tungsten promoter materials include (i) silica or thoria promoted by the oxide or a compound convertible to an oxide by calcination of tungsten or molybdenum; (ii) alumina promoted by an oxide, or compound convertible to an oxide by calcination of molybdenum or ~ 1~485~3 31722CAl tungsten; and (iii) one or more of the group aluminum phosphate, zirconiu~ phosphate, calcium phosphate, magnesium phosphate, or titanium phosphate promoted by one or more of an oxide of molybdenum or tungsten, or by a compound of molybdenum or tungsten convertible to an o~ide by calcination.
The combinations of (i), (ii), or ~iii) can be prepared and activated by suitable methods such as, ~or example, impregnation, dry mixing, or co-precipitation.
When the promoter is tungsten oxide, the preferred support material is silica or silica-containing materials. The preferred support material for molybdenum oxide is alumina or alumina-containing materials.
In general the (a) component of the catalyst system (5) will contain about 0.1 to about 30, preferably from about 1 to about 15 weight percent of the molybdenum or tungsten oxide. In addition, it is sometimes desirable that this component of the catalyst system of the invention contain relatively small amounts, from about 0.005 to about 5, preferably 0.1 to 2, weight percent of an inorganic base material. Suitable inorganic base materials include alkali metal and alkaline earth metal hydroxides and carbonates, sodium hydroxide, potassium hydroxide, sodium carbonate and potassium carbonate being preferred.
The solid (a) component of the system (5) catalysts can be in any conventional catalytic shape or size, depending upon the type of conversion in which it is to be utilized. For example, in fixed bed catalyst syste~s, the solid composite can be in the form of spheres, pellets, extrudates, agglomerates and the like. In slurry catalyst systems, the solid can be in the form of relatively small particles or in the form of a powder.
To be effective in the present catalyst system, the above-described (a) component of the catalyst system t5) is activated at elevated temperatures, generally in flowing air. The activation of the catalysts is accomplished at a temperature ranging from about 500 to 1600F for a period of several seconds to several hours. When the (a) component of the catalyst system is tungsten oxide on silica, a convenient and economical activation treatment is in the temperature range of about 900 to 1200F for a period of 15 minutes to 5 hours.
When the (a) component of the catalyst system (5) is molybdenum oxide on 7 ~Z^~S~3 31722CAI
alumina, a convenient and economical treatment is in the temperature range of about 900-1400F for 0.5 to 20 hours or longer. In some cases the activation using an oxygen-containing gas can be followed by treatment, also at elevated temperatures, with other treating gases such as carbon monoxide, hydrogen and the like.
The organoaluminum compounds which are applicable for use as the (b) component in catalyst (5) have the formula R"aAlXb where R" is a saturated aliphatic or aromatic hydrocarbon having up to about 20 carbon atoms. X is chlorine, bromine, iodine, or fluorine, a is an integer of at least 1, b can be 0, 1 or 2, and the total of a and b is 3, thus a can be 1, 2 or 3. Such aluminum compounds are well known in the art and are generally commercially available.
Some examples of suitable organoaluminum compounds halide are methylaluminum dichloride, dimethylaluminum fluoride, methylaluminum sesquichloride, trimethylaluminum, ethylaluminum dichloride, ethylaluminum sesquichloride, di(2-ethylhexyl)aluminum bromide, triisobutylaluminum, phenylaluminum dichloride, di(3 methylpentyl)aluminum bromide, cyclohexylaluminum dichloride, benzylaluminum diodide, dieicosylaluminum bromide, and the like, and mixtures thereof. The preferred (b) components are the organoaluminum halides, especially those wherein the hydrocarbon portion is an alkyl radical of 1 to 5 carbon atoms. Particularly good results are obtained with ethylaluminum dichloride, diethylaluminum chloride, and mixtures such as ethylaluminum sesquichloride and methylaluminum sesquichloride.
The molar proportion of the organoaluminum (b) component to the solid (a) component to form the catalyst system (5) useful in the practice of the present invention will generally be in the range of from about 0.005:1 to 20:1, preferably from about 0.01:1 to 10:1 moles of the (b) component per mole of the molybdenum or tungsten oxide contained in the (a) component.
It is sometimes preferred that the supported tungsten or molybdenum component, before contacting the organoaluminum compound, be treated either with nitric oxide or with a nitrosyl halide. Such treatment can take place at a temperature preferably in the range of about 0 to 130C, more preferably about 20 to 60C, for a time in the range of from a few seconds up to about 24 hours, and preferably in the ~ 317220A1 8 ~:~48543 presence of a diluent in which the nitric oxide or nitrosyl halide is at least partially soluble. After such treatment, the diluent and excess nitric oxide or nitrosyl halide can be removed from the solid catalyst by decantation, evaporation, and similar techniques. This treatment, however, should be carried out in the substantial absence of moisture, preferably in an inert atmosphere, to preserve the effects of the previous activation by calcination.
The catalyst system (5) useful in the practice of the present invention is prepared simply by combining the solid (a) component with the organoaluminum (b) component under conditions of time and temperature which permit the catalytically active catalyst composition to be formed.
The combination occurs very readily, and, in general, the components can be mixed at any convenient temperature, room temperature frequently being satisfactory, in the presence of a diluent in which the organoaluminum compound is at least partially soluble. Any convenient diluent such as, for example, benzene, cyclohexane, toluene, chiorobenzene, methylene chloride, ethylene chloride, and the like, can be used for this purpose.
Halogenated diluents are generally preferred. The mixing of these two catalyst components is carried out in the substantial absence of air or moisture, generally in an inert atmosphere. After the catalytic reaction mixture is formed, it need not be isolated but can be added directly to the olefin reaction zone as a suspension in its preparation medium. If desired, the catalyst components can be separately added, in any order, to the reaction zone either in the presence or absence of the feed olefin.
Alternatively, the system (5) catalysts useful in the practice of the invention can be separated from the preparation medium and the dissolved organoaluminum compound therein by decantation, and, after additional washing and/or drying if desired, can be added to the reaction zone as a solid rather than as a suspension.
The operating temperature for the process of this invention when using heterogeneous catalysts of (1) is in the range of about 400 to 1100F. The process of this invention when using the catalysts of (2) will be operated at a temperature in the range of about 150 to 500F.
The process using the catalysts of (3) will be carried out in a temperature range of about 600 to 1200F. The process using the 9 ~2485~3 31722CA1 catalysts of (4) will be carried out in a temperature range of about O to 600F. In the process of the invention, pressures are not important but will be generally in the range of about 0 to 2,000 psig.
According to the process of the invention employing catalyst system (5), the mixture of olefins to be converted, i.e., 1,5-cyclooctadiene and 1-hexene, is contacted with the catalyst under conditions suitable to obtain the desired reaction, for example, at a temperature in the range of about 0 to 150C and at any convenient pressure. Preferably, the temperature is in the range of about 15C to 50C wherein good results are obtained economically. Excellent results are obtained by contacting the olefin feed material with the catalyst at room temperature. The conversion can be carried out in the presence of any inert diluent such as that used for the catalyst preparation, if desired. Diluents are not essential but are sometimes preferred and such diluents can include saturated aliphatics and aromatics such as cyclohexane, xylene, isooctane, and the like, and halogenated derivatives thereof. The time of contact will depend upon the desired degree of conversion and the catalysts utilized, but will, generally, be in the range of from 0.1 minute to 24 hours, preferably 5-120 minutes. The proportion of catalyst composition to olefin feed in the reaction zone will generally be in the range of from about 0.001 to 100 millimoles of the molybdenum or tungsten oxide contained in the solid catalyst, for each mole of olefin in the reacting zone.
The oxide-promoted catalysts useful in the practice of this invention are activated by heat treatment at temperatures of from 600 to 1500F for a period of about 1 second to 25 hours or more, shorter times being used with higher temperatures and longer times with the lower temperatures. A convenient and economical treatment is obtained by subjecting the catalyst to contact with a stream of air at a temperature in the range of about 900 to 1200F for from about 15 minutes to 5 hours.
Other gases, which do not poison the catalyst, for example, nitrogen, can also be sometimes used either as a substitute for the air treatment, or as a subsequent flush. Air is usually preferred for activation, since it is readily available.
Any conventional contacting technique can be used for the olefin disproportionation employing the heterogeneous catalysts disclosed ~ 543 31722CA1 hexein, and batchwise or continuous operation can be utilized. After the reaction period, the products can be separated and/or isolated by any suitable means such as by fractionation, crystallization, adsorption, and the like. Unconverted feed materials or products not in the desired molecular weight range can be recycled to the conversion ~one. After separation of the products, the solid catalyst can be recycled to the reaction zone either with or without the addition of a fortifying amount of organoaluminum halide.
The heterogeneous catalysts employed in the practice of the invention can be further treated with modifying amounts of compounds of alkali metals or alkaline earth metals.
The catalyst supports and promoting agents employed can contain other materials which do not have a deleterious effect on the desired reaction or promote the formation of undesired by-products.
Suitable homogeneous catalysts employed in the practice of the present invention include:
(a) the coordination compounds of molybdenum or tungsten as disclosed in U.S. 3,778,385;
(b) the coordination compounds of molybdenum or tungsten complexed with N0, together with an organoaluminum adjuvant, as disclosed in U.S. 4,010,217;
(c) the neutral carbene complex catalysts disclosed in U.S. 4,247,417;
(d) the neutral carbene complex catalysts disclosed in ~.S. 4,248,738;
(e) the neutral carbene complex catalysts disclosed in U.S. 4,269,780;
(f) other homogeneous catalysts known by those of skill in the art such as, for example, WCl6+SnMe~; W(CH2C6H5)3Cl+AlCl3; WOCl4+R4Sn;
and the like.
It is also recognized by those of skill in the art that the homogeneous catalysts detailed herein can be deposited on solid support and employed as solid phase catalysts.
The metallation of 1,5,9-tetradecatriene to form 1-metallo-5,9-tetradecadiene can be carried out employing a variety of 11 ~Z48543 31722CAl metallating agents. Any metallating agent capable of selective reaction with the terminal double bond of the triene starting material is suitable. Examples of suitable metallating agents include organoboranPs, organoaluminum compounds, organomagnesium compounds, organozirconium compounds and the like.
Organoboranes contemplated to be within the scope of the present invention can be described as "hindered" organoborane compounds and can be represented by the following formula:
wherein each R is independently a Cl to C10 carbon radical wherein at least one R group is a secondary or tertiary alkyl group and each R group can be connected to the other as part of a ring structure. Exemplary compounds which satisfy the above formula include disiamylborane (i.e., bis-(3-methyl-2-butyl)borane), 9-borabicyclo [3.3.1] nonane (9-BBN), dithexylborane, thexylcyclopentylborane, thexylcyclohexylborane, and the like.
The hydroboration reaction is generally carried out in the presence of a suitable solvent such as, for example, tetrahydrofuran (THF). A roughly equimolar mixture of triene and organoborane reagent are combined. Preferably, a slight excess of triene is employed to minimize the likelihood of hydroboration occurring on the internal double bonds of the starting material triene. Typically, the hydroboration reaction should be carried out in an inert atmosphere; i.e. moisture and oxygen should be excluded from the reaction mixture. Reaction conditions employed are broadly 0-100C for a few minutes up to several hours.
Preferably, the hydroboration is carried out at about 20-80C for 15 minutes up to about 2 hours. Reaction is generally carried out at about atmospheric pressure, although higher and lower pressures are acceptable.
Once the reaction of the triene and organoboron compound is complete, the resulting 1-metallo-5,9-tetradecadiene is ready for further reaction with an appropriate C2-synthon as detailed more fully below.
Organoaluminum compounds contemplated to be within the scope of the present invention can be described by reference to the formula:
-lZ~543 31722CA1 R2AlH
wherein R is as defined above. Examples of suitable organoaluminum compounds include diisobutylaluminum hydride, diisopropylaluminum hydride and the like.
Organozirconium compounds contemplated to be within the scope of the present invention can be described by the formula:
(Ar)2Zr(X)H
wherein Ar is an aromatic ligand having 5-10 carbon atoms, such as phenyl, cyclopentadienyl, methylcyclopentadienyl, and the like, and X is a halogen. Examples of suitable organozirconium compounds include biscyclopentadienylzirconium chlorohydride, biscyclopentadienyl bromohydride, bispentamethylcyclopentadienyl chlorohydride, bismethylcyclopentadienyl chlorohydride, bisdimethylcyclopentadienyl chlorohydride, and the like.
Organomagnesium compounds contemplated to be within the scope of the present invention can be described by reference to the following formulae:
R'MgX, and R'2Mg wherein R' has at least one ~-hydrogen, and therefore is a C2 to C1O
carbon radical and X is Cl, Br or I. Exemplary compounds which satisfy the above formulae include various Grignard reagents, such as, for example, ethylmagnesium bromide, isopropylmagnesium bromide, butyl-magnesium bromide, and the like. Additional examples include dialkyl-magnesium compounds such as, for example, diethylmagnesium, diisopropyl-magnesium and the like.
Metallation with organomagnesium compounds is generally carried out in the presence of at least one transition metal activating agent.
Suitable transition metal activating agents include nickel, titanium, vanadium and zirconium compounds. Exemplary titanium activating agents include a titanocene dichloride such as, for example, dicyclopentadiene 13 1 2 g 8 5 4 3 31722CAl titanium dichloride, or alternatively, titanium tetrachloride. The molar ratio of organomagnesium compound to triene should be at least about 1:1 with the presence of a small excess of the organomagnesium compound acceptable, i.e., up to about to a 1.5 to 1 molar ratio. The molar ratio of triene to transition metal reagent is generally in the range of about 1-500:1 and preferably about 50-100:1.
Metallation with organomagnesium compounds is generally carried out at atmospheric pressure, although higher and lower pressures are operable. Preferably, atmospheric pressure or slightly reduced pressures will be employed since pressures in excess of atmospheric will tend to retard the reaction rate. Reaction temperatures of about -20 to about 100C for at least one minute up to about 24 hours are suitable.
Preferably, reaction temperature will be maintairled between about 0 and 60~C, for about 15 minutes to about 6 hours.
Conversion of the 1-metallo-5,9-tetradecadiene to a 1-substituted-7,11-hexadecadiene can be carried out by contacting the metallo-diene with a variety of C2-synthons which are reactive with the organometallic species. Exemplary reactive C2-synthons include ethylene oxide, bromoethyl acetate (BrCH2CH20COCH3), ethyl bromoacetate (BrCH2C02Et), diethyl bromomalonate, chloroethyl acetate, ethyl chloroacetate, iodoethyl acetate, ethyl iodoacetate and the like. The product is a substituted hexadecadiene or derivative thereof, which has the empirical formula, C15H27Z, wherein Z is selected from the group consisting of -CH20H, -C02CH3, and -CH20COCH3.
The 1-metallo-5,g-tetradecadiene can be contacted with an appropriate C2-synthon under suitable reaction conditions to cause the formation of a new carbon-carbon sigma bond. Thus, for example, an organoborane can be contacted with a halo-ester in the presence of a suitable base such as, for example, potassium t-butoxide. Alternatively, an organomagnesium compound can be contacted with ethylene oxide or a halo-ester, optionally in the presence of a copper (I) salt. Typical reaction conditions comprise inert atmosphere at -20 to 80C for 0.5 to 10 hours. Preferably, reaction is carried out at about -10 to +20C for 1-2 hours.
When a copper (I) salt is employed to promote the reaction of the 1-metallo-5,9-tetradecadiene and the C2 synthon, only catalytic ~Z4~S~3 31722CAl amounts are required. Thus, about 1-20 mole % copper (I) salt based on the moles of organometallic species employed are suitable. Preferably, about 2-10 mole % copper (I) salt will be used. Suitable copper (I) salts include copper (I) iodide, copper (I) bromide, copper (I) chloride and the like.
Where Z above is methoxy (-CH2OH), the product need only be esterified employing techniques well known to those of skill in the art in order to convert the hydroxy substituted hexadecadiene into gossyplure. Where Z above is acetoxy (-CO2CH3), the carbonyl function can conveniently be reduced to the alcohol by techniques known to those of skill in the art, such as, for example, reduction with lithium aluminum hydride, to give an alcohol which can then be converted to gossyplure by standard esterification techniques. Where Z is -CH20COCH3, i.e., when the C2-synthon employed is bromoethyl acetate, chloroethyl acetate or iodoethyl acetate, gossyplure is obtained directly as the product of the conversion of the l-metallo-5,9-tetradecadiene.
A further understanding of the present invention and its advantages will be provided by reference to the following examples.
Example I
Preparation of 1,5,9-Tetradecatriene a. Homogeneous catalyst Equimolar quantities of 1,5-cyclooctadiene and l-hexene were mixed in an inert atmosphere in an autoclave. The catalyst charge of about 0.0025 mole of (phenylmethoxycarbene)pentacarbonyltungsten(0) per mole of cyclooctadiene was added as a 0.1 molar solution in chlorobenzene along with approximately 0.025 mole of carbon tetrachloride as a catalyst modifier. A small amount of hexadecane (0.05-0.10 mole) was added in a precisely weighed amount as an internal standard for subsequent analysis by gas liquid chromatography (GLC).
The reaction was started and the reaction mixture was held at reaction temperature for about 2 hours after which time it was cooled, removed from the reactor and analyzed. Table I shows the results obtained from operating in the temperature range 84-92C.
iZ4~5~3 31722CA1 Table I
Preparation of 1,5,9-Tetradecatriene from 1,5-cyclooctadiene and 1-Hexene Using Homogenous (Phenylmethoxycarbene)pentacarbonyl tungsten (03 Catalyst b Selectivity Run Temp Press. CODa TDT to TDT, No. C psi Conv.,% Yield, % %
Time = 2 hrs a. COD = 1,5 Cyclooctadiene b. TDT = 1,5,9-Tetradecatriene (Phenylmethoxycarbene)pentacarbonyltungsten(O) was prepared by known literature procedures (e.g. Cardin, D. J. et al. Chem. Rev. 72 545 (1972)) b. Heterogeneous Catalyst An alumina-supported cobalt molybdate catalyst (American 20 Cyanamide HDS-20A; 78.7 wt.% Al203) was activated by heating in air at 350C for 3 hours, then under argon for about 0.5 hours, as the catalyst bed was cooled to about 130-160C for reaction. A 1:1.2 molar ratio of 1,5-cyclooctadiene:1-hexene was prepared over the above described activated catalyst at 130-160C and 4-10 weight hourly space velocity (WHSV). GLC analysis indicated about 16% conversion of cyclooctadiene feed and about 38% selectivity (or about 6% yield) to 1,5,9-tetradecatriene.
Example II
Coupling of 1,5,9-Tetradecatriene with Ethyl Bromoacetate using 9-Borabicyclononane.
1,5,9-Tetradecatriene (20 grams, 0.104 mole) in 50 mL of tetrahydrofuran was placed in a thoroughly dried 1 liter flask equipped with dropping bottle and a magnetic stirrer. An atmosphere of nitrogen was maintained in the flask. A tetrahydrofuran solution of 35 9-borabicyclononane (9-BBN) (200 mL of solution containing 0.100 mole of 9-BBN) was added slowly over about 15 minutes and the temperature was raised to reflux for 1 hour. The mixture was cooled to near 0C and 50 ~Z4859~3 mL of tertiary butyl alcohol and 17 grams of ethyl bromoacetate was added. One hundred milliliters of a 1 molar solution of potassium tertiary-butoxide and tertiary butyl alcohol was added dropwise over 0.5 hour The cloudy aqueous solution was warmed to room temperature and 33 m~ of 3 molar aqueous sodium acetate solution was added followed by 22 mL
of 30% hydrogen peroxide which was added dropwise. After stirring for an additional 30 minutes at room temperature the mixture was diluted with saturated aqueous sodium chloride and the solution was extracted with an approximately equal volume of diethyl ether. The separated ether solution was washed once with an approximately equal volume of saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate.
After filteration to remove the magnesium sulfate and simple distillation to remove the volatiles the yield was determined by GLC using a precisely weighed amount of methyl undecenoate as a standard. The results of several runs are shown in Table II.
17 lZ~8543 31722CA1 Table II
Coupling of 1,5,9-Tetradecatriene (TDT) with Ethyl Bromoacetate Using 9-Borabicyclononane (BBN) Run After TDT EHDDa 5 Run BBN Addition Conv. Yield Select No. Solvent Hrs. Temp.C % % %
4 THFb 1 reflux 64 36 56 10 6 C6C 3 reflux 92 28 30 8 C6 1 room temp. 68 27 41 9 C6/THF 1.5 50 44 17 38 THF 1 room temp. 40 8 21 15 11 C6 5.5 room temp. 51 49 95 12 C6 1 room temp. 50 45 90 14 THF 1 room temp. 48 39 81 THF 1 reflux 56 35 63 20 16 C6 5 reflux 61 44 72 a. EHDD = Ethyl Hexadecadienoate b. THF = Tetrahydrofuran c. C6 = n-Hexane It is seen that lower reaction temperatures favor higher selectivities and that longer reaction times favor higher conversions. The reasons for the inconsistencies shown such as in the extreme example in no. 10, are not known, but it is suspected that may be due to inconsistencies in excluding moisture from the potassium tertiary-butoxide solutions.
~ 8 1248543 31722CA1 Example III
Reduction of Ethylhexadecadienoate to 7,11-Hexadecadien-1-ol.
The ethylhexadecadienoate was reduced with lithium aluminum hydride (LAH) in tetrahydrofuran as follows. An oven dried 3-neck flask equipped with a magnetic stirrer, reflux condenser and an addition funnel was charged with 2 equivalents of LAH in dry tetrahydrofuran (THF). The reaction vessel and contents were maintained under a positive flow of nitrogen as 1 equivalent of ester (ethylhexadecadienoate) dissolved in an equal volume of dry THF was added dropwise to the stirred LAH suspension at a rate to maintain the THF at a gentle boil. After ester addition was complete, the reaction mixture was refluxed gently for an additional 2 hours, cooled to 0C and one equivalent of water slowly added to decompose excess LAH, followed by addition of 15% aqueous NaOH. The resulting gray gel was filtered and the organic layer washed with water, dried over adsorbent and concentrated on a rotary evaporator. Yields of about 41% of the desired 7,11-hexadecadien-1-ol were obtained.
The product alcohol was esterified without further purification.
Example IV
Acetylation of 7(Z),ll(Z,E)-Hexadecadien-1-ol Twenty-eight grams of 7,11-hexadecadien-1-ol and 50 ~L of acetic acid were reacted in 100 mL of refluxing toluene for 8 hours. The mixture was cooled, washed twice with water, once with a saturated sodium chloride solution and then dried over magnesium sulfate. The mixture was filtered, reduced in volume using a rotary evaporator and then distilled at reduced pressure through a short Vigreaux column. The gossyplure fraction boiling at 111-114C at 0.05 millimeters of mercury was collected and analyzed.
A crude yield of 54% of the gossyplure was obtained. Analysis showed that the double bond in the 11-position was about 62% trans (E) and 38% is (Z).
Example V
Coupling of 1,5,9-tetradectriene with ethylene oxide using Butylmagneium Chloride ~ 19 lZ~8~43 31722CAl 1,5,9-Tetradecatriene (lOg, 0.052 mo~; 88% purity by GLC), butylmagnesium chloride (18 mL of 2.8M in diethyl ether; 0.05 mol) and titanocene dichloride [bis(cyclopentadienyl)titanium dichloride; 0.15g, 0.6 mmol] were stirred under an inert atmosphere at room temperature.
After about three hours, the reaction mixture was cooled to about 0C and cuprous bromide (0.035 g, 0.2 mmol) and tetrahydrofuran (THF; 20 mL) were added. The reaction mixture was maintained between about 0-15C while ethylene oxide (EO; 3.2 mL, 0.063 mol~ was added slowly. Once EO
addition was complete, the reaction mixture was stirred for an additional 10 hour at 0C. Acetyl chloride (7.4 mL, 8.17 g, 0.1 mol) was then added dropwise to the reaction mixture. The reaction temperature rose to about 45C by the time acetyl chloride addition was complete. The rection mixture was stirred overnight at room temperature before workup for GLC
analysis.
Workup involved pouring the reaction mixture into an equal volume of cold water, separating and washing the organic layer with saturated sodium bicarbonate solution, drying the organic layer over MgS04, filtering and removing the solvent on a rotary evaporator. GLC
analysis indicated a 37% yield of gossyplure, based on triene starting material.
Example VI
Ten grams of 1,5(E),9(E,2)-tetradecatriene (52 mmole), 31.2 mL
of 2 molar butylmagnesium chloride (62.4 mmole) in diethyl ether and 0.65 g of titanocene dichloride (2.6 mmole) were mixed under an inert atmosphere and stirred at room temperature for two hours. The mixture was cooled to -30C and 50 mL of tetrahydrofuran was added. Cuprous bromide (2.24 g, 7.8 mmole) was added followed by ethylene oxide (63.2 mmole) which was added slowly with cooling to maintain the temperature of the reaction mixture in the range of -30 to 0C. Vigorous stirring was continued for about an hour while the temperature was held below 5C.
The product mixture was mixed first with ethyl acetate and washed with 4.5 molar HCl (about 2.5 moles HCl per mole of the starting triene), separated and then washed with a saturated aqueous sodium bicarbonate solution to remove any residual acid left in the organic layer. The yield of 7~2),11(E,Z)-hexadecadien-l-ol as determined by GLC
was 44%.
1248~43 31722C~l The 7(Z),ll(Z,E)-hexadecadien-l-ol can readily be separated by distillation. Most of the yields shown in the following tabulations were determined by GLC using a methyl silicone coated capillary column held at 80C for 2 minutes followed by temperature programmed increase of 10C/minute up to 250C.
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`S `S ~ ~J ~ `S `S ~ `S ~S ~ ~ ~ ~ ~ ~ ~ ~ D O E-l , " ~3 31722CAl The data in Table III indicate that the results are fairly consistent over more than an 80-fold increase in the scale of the reaction. Runs 1-6 show that only very small amounts of copper (I) bromide are required to produce good results in the reaction of ethylene oxide with the Grignard intermediate under the conditions used. Table IV
shows that presence of CuBr is necessary when the solvent is THF but may not be necessary in ether.
Run 40, Table V, shows that TiCl4 can be used effectively in ether solutions in place of titanocene dichloride in the transfer of MgCl0 from the butyl Grignard to the tetradecatriene moiety.
Example VII
Coupling of 1,5,9-Tetradecatriene with Bromethyl Acetate using Butylmagnesium Chloride 1,5,9-Tetradecatriene (lOg, 0.052 mol), n-butylmagnesium chloride (24.8 mL of 2.5 M in tetrahydrofuran; 0.062 mol) and titaniwn tetrachloride (0.52g, 0.0027 mol) were stirred under an inert atmosphere at about 65C for about 4.5 hours. The reaction mixture was then cooled to 0C and cuprous bromide (0.14g, 1.0 mmol) was added. 2-Bromoethyl acetate (6.9 mL, 0.063 mol) was then added dropwise and the mixture allowed to warm slowly to room temperature and stirred for several hours at room temperature. Reaction temperature was then raised to 60C for 4 hours before the mixture was cooled, acidified with aqueous HCl, then extracted with hexane. The hexane extract was washed with saturated sodium bicarbonate solution, dried over MgS04, filtered and solvent removed on the rotary evaporator. GLC analysis of this crude reaction product indicated an 11% yield of gossyplure. It should be recognized that while this reaction represents successful production of gossyplure from 1,5,9-tetradecatriene in one reaction vessel, the reaction parameters have not been optimized. Consequently, significantly improved yields of gossyplure can be expected upon optimization of various reaction parameters.
The examples have been provided merely to illustrate the practice of our invention and should not be read so as to limit the scope of our invention or the appended claims in any way. Reasonable variations and modifications, not departing from the essence and spirit ~ ~ ' 31722CAl l.Z48543 of our invention, are contemplated to be within the scope of patent protection desired and sought.
Claims (8)
1. 1-Metallo-5,9-tetradecadiene having the empirical formula C14H25M, wherein M is selected from the group consisting of MgX, MgR', BR2, AlR2, and (Ar)2Zr(X), wherein x is Cl, Br or I, each R is independently a C1 to C10 carbon radical wherein at least one R group is selected from the group consisting of secondary and ter-tiary alkyl groups, and each R can be connected to the other as part of a ring structure; R' is a C2 to C10 carbon radical and Ar is an aromatic legand having 5-10 carbon atoms.
2. A composition in accordance with claim 1 wherein said 1-metallo-5,9-tetradecadiene has the struc-ture 1-metallo-5(Z),9(Z,E)-tetradecadiene.
3. A composition in accordance with claim 1 wherein M is BR2, wherein each R is independently C1 to C10 carbon radical, wherein at least one R group is selected from the group consisting of secondary and tertiary alkyl groups, and wherein each R can be connected to the other as part of a ring structure.
4. A composition in accordance with claim 3 wherein said 1-metallo-5,9-tetradecadiene is 1-[9-borabicyclo[3.3.1]nonyl]-5,9-tetradecadiene.
5. A composition in accordance with claim 4 wherein said 1-[9-borabicyclo[3.3.1]nonyl]-5,9-tetradecadiene has the structure 1-[9-borabicyclo[3.3.1]
nonyl]-5(Z),9(Z,E)-tetradecadiene.
nonyl]-5(Z),9(Z,E)-tetradecadiene.
6. A composition in accordance with claim 1 wherein M is MgR', wherein R' is a C2 to C10 carbon radical.
7. A composition in accordance with claim 6 wherein said 1-metallo-5,9-tetradecadiene is 1-butylmag-nesium-5,9-tetradecadiene.
8. A composition in accordance with claim 7 wherein said 1-butylmagnesium-5,9-tetradecadiene has the structure 1-butylmagnesium-5(Z),9(Z,E)-tetradecadiene.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000551147A CA1248543A (en) | 1985-03-14 | 1987-11-05 | Preparation of gossyplure |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US711,891 | 1985-03-14 | ||
| US06/711,891 US4609498A (en) | 1985-03-14 | 1985-03-14 | Preparation of gossyplure |
| CA000498702A CA1241339A (en) | 1985-03-14 | 1985-12-27 | Preparation of gossyplure |
| CA000551147A CA1248543A (en) | 1985-03-14 | 1987-11-05 | Preparation of gossyplure |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000498702A Division CA1241339A (en) | 1985-03-14 | 1985-12-27 | Preparation of gossyplure |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1248543A true CA1248543A (en) | 1989-01-10 |
Family
ID=25670883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000551147A Expired CA1248543A (en) | 1985-03-14 | 1987-11-05 | Preparation of gossyplure |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA1248543A (en) |
-
1987
- 1987-11-05 CA CA000551147A patent/CA1248543A/en not_active Expired
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