US20150094481A1

US20150094481A1 - Methods of making organic compounds by metathesis and hydrocyanation

Info

Publication number: US20150094481A1
Application number: US14/512,883
Authority: US
Inventors: Timothy W. Abraham; Hiroki Kaido; Choon Woo Lee; Richard L. Pederson; Yann Schrodi; Michael John Tupy; Alexandre A. Pletnev
Original assignee: Elevance Renewable Sciences Inc
Current assignee: Materia Inc; Elevance Renewable Sciences Inc
Priority date: 2006-10-13
Filing date: 2014-10-13
Publication date: 2015-04-02
Also published as: EP2076483A4; WO2008048520A3; CN101627001A; EP2076483A2; US20090259065A1; WO2008048520A2; US8895771B2

Abstract

The invention is directed to methods of making organic compounds by metathesis and hydrocyanation. Hydrocyanation functions to introduce a nitrile group into the organic compound. The nitrile group may be converted into an amine group, an aldehyde group, an alcohol group, or a carboxylic acid group. The method of the invention may be used, for example, to make industrial important organic compounds such as diacids, diesters, acid-amines, acid-alcohols, acid-nitriles, ester-amines, ester-alcohols, and ester-nitriles.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. Ser. No. 12/422,109, which was filed Apr. 10, 2009, which is a continuation-in-part of International Application No. PCT/US2007/021931, filed Oct. 15, 2007, which claims the benefit of U.S. Provisional Application Ser. No. 60/851,367, filed Oct. 13, 2006, and entitled METHODS OF MAKING ORGANIC COMPOUNDS BY METATHESIS AND CATALYTIC MODIFICATION, the disclosures of which are incorporated herein by reference.

BACKGROUND

It is desirable to use renewable feedstocks (e.g., natural oil-derived fatty acids or fatty esters) as a source material for synthesizing industrially important organic compounds that have been conventionally manufactured from petroleum feedstocks. One useful reaction for modifying the structure of natural oil-derived feedstocks is metathesis. Metathesis is a catalytic reaction involving the rupture and reformation of carbon-carbon double bonds. When metathesis is applied directly to many natural oil-derived feedstocks, a mixture of products results. For example, when metathesis is applied to a mixture of fatty acid esters, the resulting metathesis products include a mixture of monoesters and diesters of various chain lengths. Due to the similarity in molecular weight and functionality of the products, it is difficult to separate the desired product (e.g., a particular chain length diester) from the other metathesis products. In view of the foregoing, what is desired is a method by which organic compounds may be readily synthesized from natural oil-derived feedstock materials.

SUMMARY

The invention is directed to methods of making organic compounds by metathesis and hydrocyanation. Hydrocyanation functions to introduce a nitrile group into the organic compound. The nitrile group may be converted into an amine group, an aldehyde group, an alcohol group, or a carboxylic acid group. The methods of the invention may be used to make industrial important organic compounds, for example, dicarboxylic acids (diacids), diesters, acid-amines, acid-alcohols, acid-nitriles, ester-amines, ester-alcohols, ester-nitriles, and acid-esters.
Advantageously, the method of the invention makes use of a cross-metathesis step with a short-chain olefin to chemically modify the starting composition and to produce a functionalized alkene intermediate that has a pre-determined carbon-carbon double bond position. Upon separation of the functionalized alkene intermediate, the carbon-carbon double bond is modified by hydrocyanation in order to introduce a nitrile group into the molecule. The cross-metathesis step allows the use of starting compositions that contain multiple unsaturated species (e.g., including polyunsaturated species) to produce desired organic acid compounds. Accordingly, starting compositions comprising multiple unsaturated species may be used directly in the method without prior purification.
In one aspect, the invention provides a method of making organic compounds by metathesis and catalytic modification. The method of the invention comprises the steps of:
(a) providing a starting composition comprising an unsaturated fatty acid, an unsaturated fatty ester, a salt of unsaturated fatty acid, or a mixture thereof;
(b) cross-metathesizing the starting composition of step (a) with a short-chain olefin in the presence of a metathesis catalyst to form cross-metathesis products comprising:

- (i) one or more olefin compounds; and
- (ii) an acid-, ester-, or salt-functionalized alkene having at least one carbon-carbon double bond;

(c) separating at least a portion of the acid-, ester-, or salt-functionalized alkene from the cross-metathesis products; and
(d) catalytically modifying the carbon-carbon double bond of the acid-, ester, or salt-functionalized alkene by hydrocyanation in order to introduce a nitrile group.
Useful starting compositions include unsaturated compounds (e.g., unsaturated fatty acids, unsaturated fatty esters, and carboxylate salts of unsaturated fatty acids) that are typically derived from natural oils such as vegetable oils or animal fats. In many embodiments, the starting composition comprises an unsaturated polyol ester.
When derived from a vegetable oil, useful vegetable oils include soybean oil, rapeseed oil, corn oil, sesame oil, cottonseed oil, sunflower oil, canola oil, safflower oil, palm oil, palm kernel oil, linseed oil, castor oil, olive oil, peanut oil, and mixtures thereof.
In the methods of the invention the starting composition is cross-metathesized with a short-chain olefin in the presence of a metathesis catalyst. In some embodiments, the short-chain olefin has the structure:
R⁷R⁸C═CR⁹R¹⁰
where R⁷, R⁸, R⁹, and R¹⁰are each, independently, hydrogen or an organic group, with the proviso that at least one of R⁷or R⁸is an organic group. In many embodiments, the short-chain olefin is a short-chain internal olefin. For example, the short-chain internal olefin may have the structure:
R⁷R⁸C═CR⁹R¹⁰
where R⁷, R⁸, R⁹, and R¹⁰are each, independently, hydrogen or an organic group, with the proviso that at least one of R⁷or R⁸is an organic group, and at least one of R⁹or R¹⁰is an organic group. Useful short-chain internal olefins may be symmetric or asymmetric. When symmetric, the short-chain internal olefin may have the structure:
R⁷CH═CHR⁹
where R⁷and R⁹are the same organic group. Examples of symmetric short-chain internal olefins include 2-butene, 3-hexene, and 4-octene. Examples of asymmetric short-chain internal olefin include 2-pentene, 2-hexene, 2-heptene, 3-heptene, 2-octene, 3-octene, 2-nonene, 3-nonene, and 4-nonene. In some embodiments, the short-chain olefin is an α-olefin having the structure:
CH₂═CH—R¹⁰
where —R¹⁰is an organic group. Examples of α-olefin include 1-propene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, and 1-nonene.
After cross-metathesis, at least a portion of the acid-, ester-, or salt-functionalized alkene is separated from the other cross-metathesis products. Useful separation processes include distillation, reactive distillation, chromatography, fractional crystallization, membrane separation, liquid/liquid extraction, or a combination thereof.
After separation, the carbon-carbon double bond of the separated acid-, ester, or salt-functionalized alkene is catalytically modified by hydrocyanation in order to introduce a nitrile group. After introduction of the nitrile group, the nitrile may be further reacted in order to modify the functionality of the compound. For example, in some embodiments, the nitrile group is reduced in order to convert the nitrile group into an aldehyde group or an alcohol group. In other embodiments, the nitrile group is subjected to hydrolysis in order to convert the nitrile group into a carboxylic acid. In yet other embodiments, the nitrile group is subjected to hydrogenation in order to convert the nitrile group into an amine.
In many embodiments, the organic compounds produced according to the present invention have chain lengths ranging from about 8 to 16 carbon atoms, for example, 12 carbon atoms.

DETAILED DESCRIPTION

The invention is directed to methods of making organic compounds by metathesis and hydrocyanation. The method of the invention may be used, for example, to make industrial important organic compounds such as diacids, diesters, acid-amines, acid-alcohols, acid-nitriles, ester-amines, ester-alcohols, and ester-nitriles.

Starting Composition (Step (a)):

As a starting composition, the method of the present invention uses unsaturated fatty acids, unsaturated fatty esters, salts of unsaturated fatty acids, or a mixture. As used herein the term “unsaturated fatty acid” refers to compounds that have an alkene chain with a terminal carboxylic acid group. The alkene chain may be a linear or branched and may optionally include one or more functional groups in addition to the carboxylic acid group. For example, some carboxylic acids include one or more hydroxyl groups. The alkene chain typically contains about 4 to about 30 carbon atoms, more typically about 4 to about 22 carbon atoms. In many embodiments, the alkene chain contains 18 carbon atoms (i.e., a C18 fatty acid). The unsaturated fatty acids have at least one carbon-carbon double bond in the alkene chain (i.e., a monounsaturated fatty acid), and may have more than one double bond (i.e., a polyunsaturated fatty acid) in the alkene chain. In exemplary embodiments, the unsaturated fatty acid has from 1 to 3 carbon-carbon double bonds in the alkene chain.
Also useful as starting compositions are unsaturated fatty esters. As used herein the term “unsaturated fatty ester” refers to a compounds that have an alkene chain with a terminal ester group. The alkene chain may be linear or branched and may optionally include one or more functional groups in addition to the ester group. For example, some unsaturated fatty esters include one or more hydroxyl groups in addition to the ester group. Unsaturated fatty esters include “unsaturated monoesters” and “unsaturated polyol esters”. Unsaturated monoesters have an alkene chain that terminates in an ester group, for example, an alkyl ester group such as a methyl ester. The alkene chain of the unsaturated monoesters typically contains about 4 to about 30 carbon atoms, more typically about 4 to 22 carbon atoms. In exemplary embodiments, the alkene chain contains 18 carbon atoms (i.e., a C18 fatty ester). The unsaturated monoesters have at least one carbon-carbon double bond in the alkene chain and may have more than one double bond in the alkene chain. In exemplary embodiments, the unsaturated fatty ester has 1 to 3 carbon-carbon double bonds in the alkene chain.
Also useful as a starting composition are metal salts of unsaturated fatty acids (i.e., carboxylate salts of unsaturated fatty acids). The metal salts may be salts of alkali metals (e.g., a group IA metal such as Li, Na, K, Rb, and Cs); alkaline earth metals (e.g., group IIA metals such as Be, Mg, Ca, Sr, and Ba); group IIIA metals (e.g., B, Al, Ga, In, and TI); group IVA metals (e.g., Sn and Pb), group VA metals (e.g., Sb and Bi), transition metals (e.g., Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Zr, Mo, Ru, Rh, Pd, Ag and Cd), lanthanides or actinides.
In many embodiments, the unsaturated fatty acid, ester, or carboxylate salt has a straight alkene chain and can be represented by the general formula:
CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)_n2—COOR
where:

- R is hydrogen (fatty acid), an aliphatic group (fatty ester), or a metal ion (carboxylate salt);
- n1 is an integer equal to or greater than 0 (typically 0 to 15; more typically 0, 3, or 6);
- n2 is an integer equal to or greater than 0 (typically 2 to 11; more typically 3, 4, 7, 9, or 11);
- n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 1); and
- x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).
  A summary of some unsaturated fatty acids and esters is provided in TABLE A.

TABLE A

Unsaturated Fatty Acids/Esters

		Examples	Examples
		of fatty	of fatty
Type	General Formula	acids	esters

Monounsaturated	CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)_n2—COOR	Oleic	Methyl
	Where x is 1 , and n1, n2, n3, and R are as described	Acid	Oleate
	above.	(x = 1,	(x = 1,
		n1 = 6;	n1 = 6;
		n2 = 7;	n2 = 7;
		n3 = 1;	n3 = 1;
		and R is	and R is
		H.)	CH3.)
Polyunsaturated	Diunsaturated	Linoleic	Methyl
	CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)_n2—COOR	acid	Linoleate
	Where x is 2, and n1, n2, n3, and R are as described	(x = 2,	(x = 2,
	above.	n1 = 3;	n1 = 3;
	Triunsaturated	n2 = 7;	n2 = 7;
	CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)_n2—COOR	n3 = 1;	n3 = 1;
	Where x is 3, and n1, n2, n3, and R are as described	and R is	and R is
	above.	H.)	CH3.)
		Linolenic	Methyl
		acid	Linolenate
		(x = 3,	(x = 3,
		n1 = 0;	n1 = 0;
		n2 = 7;	n2 = 7;
		n3 = 1;	n3 = 1;
		and R is	and R is
		H.)	CH3.)

Unsaturated monoesters may be alkyl esters (e.g., methyl esters) or aryl esters and may be derived from unsaturated fatty acids by esterification, or unsaturated glycerides by transesterifying, with a monohydric alcohol. The monohydric alcohol may be any monohydric alcohol that is capable of reacting with the unsaturated free fatty acid or unsaturated glyceride to form the corresponding unsaturated monoester. In some embodiments, the monohydric alcohol is a C1 to C20 monohydric alcohol, for example, a C1 to C12 monohydric alcohol, a C1 to C8 monohydric alcohol, or a C1 to C4 monohydric alcohol. The carbon atoms of the monohydric alcohol may be arranged in a straight chain or in a branched chain structure, and may be substituted with one or more substituents. Representative examples of monohydric alcohols include methanol, ethanol, propanol (e.g., isopropanol), and butanol.
Transesterification of an unsaturated triglyceride can be represented as follows.
1 Unsaturated Triglyceride+3 Alcohol→1 Glycerol+3 Monoesters
Depending upon the make-up of the unsaturated triglyceride, the above reaction may yield one, two, or three moles of unsaturated monoester. Transesterification is typically conducted in the presence of a catalyst, for example, alkali catalysts, acid catalysts, or enzymes. Representative alkali transesterification catalysts include NaOH, KOH, sodium and potassium alkoxides (e.g., sodium methoxide), sodium ethoxide, sodium propoxide, sodium butoxide. Representative acid catalysts include sulfuric acid, phosphoric acid, hydrochloric acid, and sulfonic acids. Heterogeneous catalysts may also be used for transesterification. These include alkaline earth metals or their salts such as CaO, MgO, calcium acetate, barium acetate, natural clays, zeolites, Sn, Ge or Pb, supported on various materials such as ZnO, MgO, TiO₂, activated carbon or graphite, and inorganic oxides such as alumina, silica-alumina, boria, oxides of P, Ti, Zr, Cr, Zn, Mg, Ca, and Fe. In exemplary embodiments, the triglyceride is transesterified with methanol (CH₃OH) in order to form free fatty acid methyl esters.
In some embodiments, the unsaturated fatty esters are unsaturated polyol esters. As used herein the term “unsaturated polyol ester” refers to compounds that have at least one unsaturated fatty acid that is esterified to the hydroxyl group of a polyol. The other hydroxyl groups of the polyol may be unreacted, may be esterified with a saturated fatty acid, or may be esterified with an unsaturated fatty acid. The fatty acids in the polyol ester may be linear or branched and may optionally have functional groups other than the carboxylic acid such as one or more hydroxyl groups. Examples of polyol include glycerol, 1,3-propanediol, 1,2-propenediol, ethylene glycol, 1,4-butanediol, 2,3-butanediol, 1,6-hexanediol, 1,5-pentanediol, trimethylolpropane, erythritol, pentaerythritol, and sorbitol. In many embodiments, unsaturated polyol esters have the general formula:
R(O—Y)_m(OH)_n(O—X)_b
where

- R is an organic group having a valency of (n+m+b);
- m is an integer from 0 to (n+m+b−1), typically 0 to 2;
- b is an integer from 1 to (n+m+b), typically 1 to 3;
- n is an integer from 0 to (n+m+b−1), typically 0 to 2;
- (n+m+b) is an integer that is 2 or greater;
- X is —(O)C—(CH₂)_n2—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃;
- Y is —(O)C—R′;
- R′ is a straight or branched chain alkyl or alkenyl group;
- n1 is an integer equal to or greater than 0 (typically 0 to 15; more typically 0, 3, or 6);
- n2 is an integer equal to or greater than 0 (typically 2 to 11; more typically 3, 4, 7, 9, or 11);
- n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 1); and
- x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

In many embodiments, the unsaturated polyol esters are unsaturated glycerides. As used herein the term “unsaturated glyceride” refers to a polyol ester having at least one (e.g., 1 to 3) unsaturated fatty acid that is esterified with a molecule of glycerol. The fatty acid groups may be linear or branched and may include pendant hydroxyl groups. In many embodiments, the unsaturated glycerides are represented by the general formula:
CH₂A-CHB—CH₂C

- where -A; —B; and —C are selected from
  - —OH;
  - —O(O)C—(CH₂)_n2—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃; and
  - —O(O)C—R′;
- with the proviso that at least one of -A, —B, or —C is
  - —O(O)C—(CH₂)_n2—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃.
- In the above formula:
  - R′ is a straight or branched chain alkyl or alkenyl group;
  - n1 is an integer equal to or greater than 0 (typically 0 to 15; more typically 0, 3, or 6);
  - n2 is an integer equal to or greater than 0 (typically 2 to 11; more typically 3, 4, 7, 9, or 11);
  - n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 1); and
  - x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

Unsaturated glycerides having two —OH groups (e.g., -A and —B are —OH) are commonly known as unsaturated monoglycerides. Unsaturated glycerides having one —OH group are commonly known as unsaturated diglycerides. Unsaturated glycerides having no —OH groups are commonly known as unsaturated triglycerides.
As shown in the formula above, the unsaturated glyceride may include monounsaturated fatty acids, polyunsaturated fatty acids, and saturated fatty acids that are esterified to the glycerol molecule. The main chain of the individual fatty acids may have the same or different chain lengths. Accordingly, the unsaturated glyceride may contain up to three different fatty acids so long as at least one fatty acid is an unsaturated fatty acid.
In many embodiments, useful starting compositions are derived from natural oils, such as plant-based oils, animal fats, or algae oils. Representative examples of plant-based oils include canola oil, rapeseed oil, coconut oil, corn oil, cottonseed oil, olive oil, palm oil, peanut oil, safflower oil, sesame oil, soybean oil, sunflower oil, linseed oil, palm kernel oil, tung oil, castor oil, tall oil, and the like. Representative examples of animal fats include lard, tallow, chicken fat (yellow grease), and fish oil.
In many embodiments, the plant-based oil is soybean oil. Soybean oil comprises unsaturated glycerides, for example, in many embodiments about 95% weight or greater (e.g., 99% weight or greater) triglycerides. Major fatty acids making up soybean oil include saturated fatty acids, for example, palmitic acid (hexadecanoic acid) and stearic acid (octadecanoic acid), and unsaturated fatty acids, for example, oleic acid (9-octadecenoic acid), linoleic acid (9,12-octadecadienoic acid), and linolenic acid (9,12,15-octadecatrienoic acid). Soybean oil is a highly unsaturated vegetable oil with many of the triglyceride molecules having at least two unsaturated fatty acids.
The method of the invention can be used to produce multiple organic acid compounds. As discussed below, the position of the carbon-carbon double bond closest to the carboxylic acid, ester, or carboxylate salt group dictates the chain length of the organic acid compound that is formed by the method of the invention.

Δ9 Starting Compositions:

In many embodiments, the starting composition comprises a Δ9 unsaturated fatty acid, a Δ9 unsaturated fatty ester (e.g., monoesters or polyol esters), a Δ9 unsaturated fatty acid salt, or a mixture of two or more of the foregoing. Δ9 unsaturated starting materials have a carbon-carbon double bond located between the 9^thand 10^thcarbon atoms (i.e., between C9 and C10) in the alkene chain of the unsaturated fatty acid, ester, or salt. In determining this position, the alkene chain is numbered beginning with the carbon atom in the carbonyl group of the unsaturated fatty acid, ester, or salt. Δ9 unsaturated fatty acids, esters, and salts include polyunsaturated fatty acids, esters, or salts (i.e., having more than one carbon-carbon double bond in the alkene chain) so long as one of the carbon-carbon double bonds is located between C9 and C10. For example, included within the definition of Δ9 unsaturated fatty acids, esters, or salts are Δ9, 12 unsaturated fatty acids, esters or salts, and Δ9, 12, 15 unsaturated fatty acids, esters or salts.
In many embodiments, the Δ9 unsaturated starting materials have a straight alkene chain and may be represented by the general structure:
CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)₇—COOR
where

- R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt);
- n1 is an integer equal to or greater than 0 (typically 0 to 6; more typically 0, 3, 6);
- n3 is an integer equal to or greater than 0 (typically 1); and
- x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

In exemplary embodiments, the Δ9 unsaturated starting materials have a total of 18 carbons in the alkene chain. Examples include
CH₃—(CH₂)₇—CH═CH—(CH₂)₇—COOR;
CH₃—(CH₂)₄—CH═CH—CH₂—CH═CH—(CH₂)₇—COOR; and
CH₃—CH₂—CH═CH—CH₂—CH═CH—CH₂—CH═CH—(CH₂)₇—COOR.

- where R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (fatty acid salt);

Δ9 unsaturated fatty esters may be monoesters or polyol esters. In many embodiments, the Δ9 unsaturated polyol esters have the general structure:
CH₂A-CHB—CH₂C

- where -A; —B; and —C are independently selected from
  - —OH;
  - —O(O)C—R′; and
  - —O(O)C—(CH₂)₇—[—CH═CH—(CH₂)_n3—]_x-—(CH₂)_n1—CH₃;
- with the proviso that at least one of -A, —B, or —C is
  - —O(O)C—(CH₂)₇—[—CH═CH—(CH₂)_n3—]_x-—(CH₂)_n1—CH₃.
- In the above formula:
  - R′ is a straight or branched chain alkyl or alkenyl group;
  - n1 is an integer equal to or greater than 0 (typically 0 to 6; more typically 0, 3, 6);
  - n3 is an integer equal to or greater than 0 (typically 1); and
  - x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

In exemplary embodiments, the starting composition comprises one or more C18 fatty acids, for example, oleic acid (i.e., 9-octadecenoic acid), linoleic acid (i.e., 9,12-octadecadienoic acid), and linolenic acid (i.e., 9,12,15-octadecatrienoic acid). In other exemplary embodiments, the starting composition comprises one or more C18 fatty esters, for example, methyl oleate, methyl linoleate, and methyl linolenate. In yet another exemplary embodiment, the starting composition comprises an unsaturated glyceride comprising Δ9 fatty acids, for example, C18 Δ9 fatty acids.
Δ9 starting compositions may be derived, for example, from vegetable oils such as soybean oil, rapeseed oil, corn oil, sesame oil, cottonseed oil, sunflower oil, canola oil, safflower oil, palm oil, palm kernel oil, linseed oil, castor oil, olive oil, peanut oil, and the like. Since these vegetable oils yield predominately in glyceride form, the oils are typically processed (e.g., by transesterification) to yield unsaturated fatty esters, unsaturated free fatty acids, or carboxylate salts thereof. Δ9 starting materials may also be derived from tung oil which typically contains oleic acid, linoleic acid, and elostearic acid (C18; Δ9, 11, 13) in glyceride form. Δ9 starting materials may also be derived from tall oil, fish oil, lard, and tallow.

Δ5 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ5 unsaturated fatty acids, esters, or salts. As used herein “Δ5” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 5th and 6th carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ5 unsaturated fatty acids, esters, and salts have the general structure:
CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)₃—COOR
where

- R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt);
- n1 is an integer equal to or greater than 0 (typically 1 to 15; more typically 1, 13, or 15);
- n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 0 or 6); and
- x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 2).

The Δ5 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ5 unsaturated polyol esters have the general structure:
CH₂A-CHB—CH₂C

- where -A; —B; and —C are independently selected from
  - —OH;
  - —O(O)C—R′; and
  - —O(O)C—(CH₂)₃—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃;
- with the proviso that at least one of -A, —B, or —C is
  - —O(O)C—(CH₂)₃—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1CH₃.
- In the above formula:
  - R′ is a straight or branched chain alkyl or alkenyl group;
  - n1 is an integer equal to or greater than 0 (typically 1 to 15; more typically 1, 13, or 15);
  - n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 0 or 6); and
  - x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 2).

Δ5 starting compositions may be derived, for example, from meadowfoam oil which contains a twenty carbon monounsaturated fatty acid (C20:1; Δ5) in glyceride form. Δ5 starting compositions may also be derived from fish oil which typically contains eicosapentaenoic acid (C20:5; Δ5, 8, 11, 14, 17) in glyceride form.

Δ6 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ6 unsaturated fatty acids, esters, or salts. As used herein “Δ6” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 6th and 7th carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ6 unsaturated fatty acids, esters, and salts have the general structure:
CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)₄—COOR
where

- R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt);
- n1 is an integer equal to or greater than 0 (typically 0 to 10);
- n3 is an integer equal to or greater than 0; (typically 0); and
- x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

The Δ6 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ6 unsaturated polyol esters have the general structure:
CH₂A-CHB—CH₂C

- where -A; —B; and —C are independently selected from
  - —OH;
  - —O(O)C—R′; and
  - —O(O)C—(CH₂)₄—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃;
- with the proviso that at least one of -A, —B, or —C is
  - —O(O)C—(CH₂)₄—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃.
- In the above formula:
  - R′ is a straight or branched chain alkyl or alkenyl group;
  - n1 is an integer equal to or greater than 0 (typically 0 to 10);
  - n3 is an integer equal to or greater than 0; (typically 0); and
  - x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

Δ6 starting compositions may be derived from coriander oil which contains an 18 carbon unsaturated fatty acid (C18:1; Δ6) in glyceride form.

Δ11 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ11 unsaturated fatty acids, esters, or salts. As used herein “Δ11” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 11^thand 12^thcarbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ11 unsaturated fatty acids, esters, and salts have the general structure:
CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)₉—COOR
where

- R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt);
- n1 is an integer equal to or greater than 0 (typically 0 to 7; more typically 7);
- n3 is an integer equal to or greater than 0 (typically 0); and
- x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

The Δ11 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ11 unsaturated polyol esters have the general structure:
CH₂A-CHB—CH₂C

- where -A; —B; and —C are independently selected from
- —OH;
  - —O(O)C—R′; and
  - —O(O)C—(CH₂)₉—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1CH₃;
- with the proviso that at least one of -A, —B, or —C is
  - —O(O)C—(CH₂)₉—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1CH₃.
- In the above formula:
  - R′ is a straight or branched chain alkyl or alkenyl group;
  - n1 is an integer equal to or greater than 0 (typically 0 to 7; more typically 7);
  - n3 is an integer equal to or greater than 0 (typically 0); and
  - x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

Sources of Δ11 starting compositions include camelina oil which contains gondoic acid (C20:1 Δ11) at approximately 15% of the fatty acid composition.

Δ13 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are Δ13 unsaturated fatty acids, esters, or salts. As used herein “Δ13” refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 13^thand 14^thcarbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, Δ13 unsaturated fatty acids, esters, and salts have the general structure:
CH₃—(CH₂)_n1—[—(CH₂)_n3—CH═CH—]_x—(CH₂)₁₁—COOR
where

- R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt);
- n1 is an integer equal to or greater than 0 (typically 7);
- n3 is an integer equal to or greater than 0 (typically 0)
- x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

The Δ13 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the Δ13 unsaturated polyol esters have the general structure
CH₂A-CHB—CH₂C

- where -A; —B; and —C are independently selected from
  - —OH;
  - —O(O)C—R′; and
  - —O(O)C—(CH₂)₁₁—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃;
- with the proviso that at least one of -A, —B, or —C is
  - —O(O)C—(CH₂)₁₁—[—CH═CH—(CH₂)_n3—]_x—(CH₂)_n1—CH₃.
- In the above formula:
  - R′ is a straight or branched chain alkyl or alkenyl group;
  - n1 is an integer equal to or greater than 0 (typically 7);
  - n3 is an integer equal to or greater than 0 (typically 0)
  - x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

Sources of Δ13 starting compositions include crambe oil, fish oil, and high erucic acid rapeseed oil which are high in erucic acid (C22:1 Δ13) in glyceride form.
Other useful starting compositions include, for example, Δ8 and Δ4 starting materials. Δ4 starting materials may be obtained, for example, from fish oil which typically includes an amount of docosahexaenoic acid (C22:6; Δ4, 7, 10, 13, 16, 19). Δ8 starting materials may also be obtained from fish oil which typically includes an amount of eicosatetraenoic acid (C20:4; Δ8, 11, 14, 17).
A summary of some useful starting compositions is provided in TABLE B.

TABLE B

Starting		Classi-	Bond
Composition	Description	fication	Locations

Oleic acid	C18 monounsaturated fatty	Δ9	Δ9
	acid (C18:1)
Linoleic acid	C18 diunsaturated fatty	Δ9	Δ9, 12
	acid (C18:2)
Linolenic acid	C18 triunsaturated fatty	Δ9	Δ9, 12, 15
	acid (C18:3)
Alkyl oleate	C18 monounsaturated fatty	Δ9	Δ9
	ester (C18:1)
Alkyl linoleate	C18 diunsaturated fatty	Δ9	Δ9, 12
	ester (C18:2)
Alkyl linolenate	C18 triunsaturated fatty	Δ9	Δ9, 12, 15
	ester (C18:3)
Vegetable Oil	Unsaturated glycerides of	Δ9	Δ9
(e.g., soybean oil)	C18:1, C18:2, and C18:3		Δ9, 12
	fatty acids		Δ9, 12, 15
Tung Oil	Unsaturated glycerides of	Δ9	Δ9, 11, 13
	C18:1; C18:2; and C18:3		Δ9
	fatty acids		Δ9, 12
Meadowfoam Oil	Unsaturated glycerides of	Δ5	Δ5
	C20:1 fatty acids.
Coriander Oil	Unsaturated glycerides of	Δ6	Δ6
	C18:1 fatty acids.
Camelina oil	Unsaturated glycerides of	Δ11	Δ11
	C20:1 fatty acids
Crambe Oil or	Unsaturated glycerides of	Δ13	Δ13
High Erucic	C22:1 fatty acids
Rapeseed Oil

Cross-Metathesis (Step (b)):

In the method of the present invention, the starting composition is cross-metathesized with an alpha olefin, an internal olefin, or a mixture thereof, to form cross-metathesis products comprising: (i) one or more olefins; and (ii) one or more acid-, ester-, or salt-functionalized alkenes.
In some embodiments, the internal olefin is a short-chain olefin (“SCO”). Short-chain olefins are short-chain length organic compounds that have at least one carbon-carbon double bond. Typically, the short-chain length internal olefins have between about 4 and about 9 carbon atoms. Short-chain olefins can be represented by the structure (II):
R⁷R⁸C═CR⁹R¹⁰ (II)

- where R⁷, R⁸, R⁹, and R¹⁰are each, independently, hydrogen or an organic group, with the proviso that at least one of R⁷or R⁸is an organic group.

The organic group may be an aliphatic group, an alicyclic group or an aromatic group. Organic groups may optionally include heteroatoms (e.g., O, N, or S atoms), as well as functional groups (e.g., carbonyl groups). The term aliphatic group means a saturated or unsaturated, linear or branched, hydrocarbon group. This term is used to encompass alkyl groups. The term alkyl group means a monovalent, saturated, linear, branched, or cyclic hydrocarbon group. Representative examples include of alkyl groups include methyl, ethyl, propyl (n-propyl or i-propyl)butyl (n-butyl or t-butyl), and heptyl. An alicyclic group is an aliphatic group arranged in one or more closed ring structures. The term is used to encompass saturated (i.e., cycloparaffins) or unsaturated (cycloolefins or cycloacetylenes) groups. An aromatic or aryl group is an unsaturated cyclic hydrocarbon having a conjugated ring structure. Included within aromatic or aryl groups are those possessing both an aromatic ring structure and an aliphatic or alicyclic group.
In some embodiments, the short-chain olefin is a short-chain internal olefin. Short-chain internal olefins may be represented by structure (II) where R⁷, R⁸, R⁹, and R¹⁰are each, independently, hydrogen or an organic group, with the proviso that at least one of R⁷or R⁸is an organic group, and at least one of R⁹or R¹⁰is an organic group.
Short-chain internal olefins may be symmetric or asymmetric. Symmetric short-chain internal olefins having one carbon-carbon double bond may be represented by structure (II-A):
R⁷CH═CHR⁹ (II-A)

- where R⁷and R⁹are same organic group.

Representative examples of symmetric short-chain internal olefins include 2-butene, 3-hexene, and 4-octene. In some embodiments, the short-chain internal olefin is asymmetric. Representative examples of asymmetric short-chain internal olefins include 2-pentene, 2-hexene, 2-heptene, 3-heptene, 2-octene, 3-octene, 2-nonene, 3-nonene, and 4-nonene.
In many embodiments, symmetric short-chain internal olefins are preferred for cross-metathesis because the cross-metathesis products that result will include fewer products than if an asymmetric short-chain internal olefin is used for cross-metathesis. For example, as shown below, when a first double-bond containing compound (i.e., A=B) is cross-metathesized with a symmetric short-chain internal olefin (i.e., represented by C═C), two cross-metathesis products are produced. By contrast, when the same double-bond containing compound is cross-metathesisized with an asymmetric short-chain internal olefin (i.e., represented by C=D), four cross-metathesis products are produced.

- Metathesis of Symmetric Short-chain Internal Olefin (C═C)

A=B+C═C
A=C+B═C

- Metathesis of Asymmetric Short-chain Internal Olefin (C=D):

A=B+C=D
A=C+B═C+A=D+B=D
In some embodiments, the short-chain olefin is an α-olefin. Alpha olefins are included in general structure (II) when R⁷, R⁸, and R⁹are all hydrogen. Representative α-olefin are shown in general structure (II-B):
CH₂═CH—R¹⁰ (II-B)

- where R¹⁰is an organic group.

Representative —R¹⁰groups include —CH₃and —(CH₂)_n—CH₃, where n ranges from 0 to 6. Exemplary alpha olefin compounds include 1-propene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, and 1-nonene.

Metathesis Catalysts:

The metathesis reaction is conducted in the presence of a catalytically effective amount of a metathesis catalyst. The term “metathesis catalyst” includes any catalyst or catalyst system which catalyzes the metathesis reaction.
Any known or future-developed metathesis catalyst may be used, alone or in combination with one or more additional catalysts, in accordance with embodiments of the present method. Exemplary metathesis catalysts include metal carbene catalysts based upon transition metals, for example, ruthenium, molybdenum, osmium, chromium, rhenium, and tungsten. In certain embodiments, the metathesis catalyst is preferably a Group 8 transition metal complex having the structure of formula (III)
in which the various substituents are as follows:

- M is a Group 8 transition metal;
- L¹, L²and L³are neutral electron donor ligands;
- n is 0 or 1, such that L³may or may not be present;
- m is 0, 1, or 2;
- X¹and X²are anionic ligands; and
- R¹and R²are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and functional groups,
- wherein any two or more of X¹, X², L¹, L², L³, R¹, and R²can be taken together to form a cyclic group, and further wherein any one or more of X¹, X², L¹, L², L³, R¹, and R²may be attached to a support.

Preferred catalysts contain Ru or Os as the Group 8 transition metal, with Ru particularly preferred.
Numerous embodiments of the catalysts useful in the reactions of the disclosure are described in more detail infra. For the sake of convenience, the catalysts are described in groups, but it should be emphasized that these groups are not meant to be limiting in any way. That is, any of the catalysts useful in the disclosure may fit the description of more than one of the groups described herein.
A first group of catalysts, then, are commonly referred to as 1^stGeneration Grubbs-type catalysts, and have the structure of formula (III). For the first group of catalysts, M and m are as described above, and n, X¹, X², L¹, L², L³, R¹, m and R²are described as follows.
For the first group of catalysts, n is 0, and L¹and L²are independently selected from phosphine, sulfonated phosphine, phosphite, phosphinite, phosphonite, arsine, stibine, ether, amine, amide, imine, sulfoxide, carboxyl, nitrosyl, pyridine, substituted pyridine, imidazole, substituted imidazole, pyrazine, and thioether. Exemplary ligands are trisubstituted phosphines.
X¹and X²are anionic ligands, and may be the same or different, or are linked together to form a cyclic group, typically although not necessarily a five- to eight-membered ring. In preferred embodiments, X¹and X²are each independently hydrogen, halide, or one of the following groups: C₁-C₂₀alkyl, C₅-C₂₄aryl, C₁-C₂₀alkoxy, C₅-C₂₄aryloxy, C₂-C₂₀alkoxycarbonyl, C₆-C₂₄aryloxycarbonyl, C₂-C₂₄acyl, C₂-C₂₄acyloxy, C₁-C₂₀alkylsulfonato, C₅-C₂₄arylsulfonato, C₁-C₂₀alkylsulfanyl, C₅-C₂₄arylsulfanyl, C₁-C₂₀alkylsulfinyl, or C₅-C₂₄arylsulfinyl. Optionally, X¹and X²may be substituted with one or more moieties selected from C₁-C₁₂alkyl, C₁-C₁₂alkoxy, C₅-C₂₄aryl, and halide, which may, in turn, with the exception of halide, be further substituted with one or more groups selected from halide, C₁-C₆alkyl, C₁-C₆alkoxy, and phenyl. In more preferred embodiments, X¹and X²are halide, benzoate, C₂-C₆acyl, C₂-C₆alkoxycarbonyl, C₁-C₆alkyl, phenoxy, C₁-C₆alkoxy, C₁-C₆alkylsulfanyl, aryl, or C₁-C₆alkylsulfonyl. In even more preferred embodiments, X¹and X²are each halide, CF₃CO₂, CH₃CO₂, CFH₂CO₂, (CH₃)₃CO, (CF₃)₂(CH₃)CO, (CF₃)(CH₃)₂CO, PhO, MeO, EtO, tosylate, mesylate, or trifluoromethane-sulfonate. In the most preferred embodiments, X¹and X²are each chloride.
R¹and R²are independently selected from hydrogen, hydrocarbyl (e.g., C₁-C₂₀alkyl, C₂-C₂₀alkenyl, C₂-C₂₀alkynyl, C₅-C₂₄aryl, C₆-C₂₄alkaryl, C₆-C₂₄aralkyl, etc.), substituted hydrocarbyl (e.g., substituted C₁-C₂₀alkyl, C₂-C₂₀alkenyl, C₂-C₂₀alkynyl, C₅-C₂₄aryl, C₆-C₂₄alkaryl, C₆-C₂₄aralkyl, etc.), heteroatom-containing hydrocarbyl (e.g., heteroatom-containing C₁-C₂₀alkyl, C₂-C₂₀alkenyl, C₂-C₂₀alkynyl, C₅-C₂₄aryl, C₆-C₂₄alkaryl, C₆-C₂₄aralkyl, etc.), and substituted heteroatom-containing hydrocarbyl (e.g., substituted heteroatom-containing C₁-C₂₀alkyl, C₂-C₂₀alkenyl, C₂-C₂₀alkynyl, C₅-C₂₄aryl, C₆-C₂₄alkaryl, C₆-C₂₄aralkyl, etc.), and functional groups. R¹and R²may also be linked to form a cyclic group, which may be aliphatic or aromatic, and may contain substituents and/or heteroatoms. Generally, such a cyclic group will contain 4 to 12, preferably 5, 6, 7, or 8 ring atoms.
In preferred catalysts, R¹is hydrogen and R²is selected from C₁-C₂₀alkyl, C₂-C₂₀alkenyl, and C₅-C₂₄aryl, more preferably C₁-C₆alkyl, C₂-C₆alkenyl, and C₅-C₁₄aryl. Still more preferably, R²is phenyl, vinyl, methyl, isopropyl, or t-butyl, optionally substituted with one or more moieties selected from C₁-C₆alkyl, C₁-C₆alkoxy, phenyl, and a functional group Fn as defined earlier herein. Most preferably, R²is phenyl or vinyl substituted with one or more moieties selected from methyl, ethyl, chloro, bromo, iodo, fluoro, nitro, dimethylamino, methyl, methoxy, and phenyl. Optimally, R²is phenyl or —C═C(CH₃)₂.
Any two or more (typically two, three, or four) of X¹, X², L¹, L², L³, R¹, and R²can be taken together to form a cyclic group, as disclosed, for example, in U.S. Pat. No. 5,312,940 to Grubbs et al. When any of X¹, X², L¹, L², L³, R¹, and R²are linked to form cyclic groups, those cyclic groups may contain 4 to 12, preferably 4, 5, 6, 7 or 8 atoms, or may comprise two or three of such rings, which may be either fused or linked. The cyclic groups may be aliphatic or aromatic, and may be heteroatom-containing and/or substituted. The cyclic group may, in some cases, form a bidentate ligand or a tridentate ligand. Examples of bidentate ligands include, but are not limited to, bisphosphines, dialkoxides, alkyldiketonates, and aryldiketonates.
A second group of catalysts, commonly referred to as 2^ndGeneration Grubbs-type catalysts, have the structure of formula (III), wherein L¹is a carbene ligand having the structure of formula (IV)
such that the complex may have the structure of formula (V)
wherein M, m, n, X¹, X², L², L³, R¹, and R²are as defined for the first group of catalysts, and the remaining substituents are as follows.
X and Y are heteroatoms typically selected from N, O, S, and P. Since O and S are divalent, p is necessarily zero when X is O or S, and q is necessarily zero when Y is O or S. However, when X is N or P, then p is 1, and when Y is N or P, then q is 1. In a preferred embodiment, both X and Y are N.
Q¹, Q², Q³, and Q⁴are linkers, e.g., hydrocarbylene (including substituted hydrocarbylene, heteroatom-containing hydrocarbylene, and substituted heteroatom-containing hydrocarbylene, such as substituted and/or heteroatom-containing alkylene) or —(CO)—, and w, x, y, and z are independently zero or 1, meaning that each linker is optional. Preferably, w, x, y, and z are all zero. Further, two or more substituents on adjacent atoms within Q¹, Q², Q³, and Q⁴may be linked to form an additional cyclic group.
R³, R^3A, R⁴, and R^4Aare independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl.
In addition, any two or more of X¹, X², L¹, L², L³, R¹, R², R³, R^3A, R⁴, and R^4Acan be taken together to form a cyclic group, and any one or more of X¹, X², L¹, L², L³, R¹, R², R³, R^3A, R⁴, and R^4Amay be attached to a support.
Preferably, R^3Aand R^4Aare linked to form a cyclic group so that the carbene ligand is an heterocyclic carbene and preferably an N-heterocyclic carbene, such as the N-heterocylic carbene having the structure of formula (VI):
where R³and R⁴are defined above, with preferably at least one of R³and R⁴, and more preferably both R³and R⁴, being alicyclic or aromatic of one to about five rings, and optionally containing one or more heteroatoms and/or substituents. Q is a linker, typically a hydrocarbylene linker, including substituted hydrocarbylene, heteroatom-containing hydrocarbylene, and substituted heteroatom-containing hydrocarbylene linkers, wherein two or more substituents on adjacent atoms within Q may also be linked to form an additional cyclic structure, which may be similarly substituted to provide a fused polycyclic structure of two to about five cyclic groups. Q is often, although again not necessarily, a two-atom linkage or a three-atom linkage.
Examples of N-heterocyclic carbene ligands suitable as L¹thus include, but are not limited to, the following:
When M is ruthenium, then, the preferred complexes have the structure of formula (VII).
In a more preferred embodiment, Q is a two-atom linkage having the structure —CR¹¹R¹²—CR¹³R¹⁴— or —CR¹¹═CR¹³—, preferably —CR¹¹R¹²—CR¹³R¹⁴—, wherein R¹¹, R¹², R¹³, and R¹⁴are independently selected from hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and functional groups. Examples of functional groups here include carboxyl, C₁-C₂₀alkoxy, C₅-C₂₄aryloxy, C₂-C₂₀alkoxycarbonyl, C₅-C₂₄alkoxycarbonyl, C₂-C₂₄acyloxy, C₁-C₂₀alkylthio, C₅-C₂₄arylthio, C₁-C₂₀alkylsulfonyl, and C₁-C₂₀alkylsulfinyl, optionally substituted with one or more moieties selected from C₁-C₁₂alkyl, C₁-C₁₂alkoxy, C₅-C₁₄aryl, hydroxyl, sulfhydryl, formyl, and halide. R¹¹, R¹², R¹³, and R¹⁴are preferably independently selected from hydrogen, C1-C12 alkyl, substituted C₁-C₁₂alkyl, C₁-C₁₂heteroalkyl, substituted C₁-C₁₂heteroalkyl, phenyl, and substituted phenyl. Alternatively, any two of R¹¹, R¹², R¹³, and R¹⁴may be linked together to form a substituted or unsubstituted, saturated or unsaturated ring structure, e.g., a C₄-C₁₂alicyclic group or a C₅or C₆aryl group, which may itself be substituted, e.g., with linked or fused alicyclic or aromatic groups, or with other substituents.
When R³and R⁴are aromatic, they are typically although not necessarily composed of one or two aromatic rings, which may or may not be substituted, e.g., R³and R⁴may be phenyl, substituted phenyl, biphenyl, substituted biphenyl, or the like. In one preferred embodiment, R³and R⁴are the same and are each unsubstituted phenyl or phenyl substituted with up to three substituents selected from C₁-C₂₀alkyl, substituted C₁-C₂₀alkyl, C₁-C₂₀heteroalkyl, substituted C₁-C₂₀heteroalkyl, C₅-C₂₄aryl, substituted C₅-C₂₄aryl, C₅-C₂₄heteroaryl, C₆-C₂₄aralkyl, C₆-C₂₄alkaryl, or halide. Preferably, any substituents present are hydrogen, C₁-C₁₂alkyl, C₁-C₁₂alkoxy, C₅-C₁₄aryl, substituted C₅-C₁₄aryl, or halide. As an example, R³and R⁴are mesityl.
In a third group of catalysts having the structure of formula (III), M, m, n, X¹, X², R¹, and R²are as defined for the first group of catalysts, L¹is a strongly coordinating neutral electron donor ligand such as any of those described for the first and second groups of catalysts, and L²and L³are weakly coordinating neutral electron donor ligands in the form of optionally substituted heterocyclic groups. Again, n is zero or 1, such that L³may or may not be present. Generally, in the third group of catalysts, L²and L³are optionally substituted five- or six-membered monocyclic groups containing 1 to 4, preferably 1 to 3, most preferably 1 to 2 heteroatoms, or are optionally substituted bicyclic or polycyclic structures composed of 2 to 5 such five- or six-membered monocyclic groups. If the heterocyclic group is substituted, it should not be substituted on a coordinating heteroatom, and any one cyclic moiety within a heterocyclic group will generally not be substituted with more than 3 substituents.
For the third group of catalysts, examples of L²and L³include, without limitation, heterocycles containing nitrogen, sulfur, oxygen, or a mixture thereof.
Examples of nitrogen-containing heterocycles appropriate for L²and L³include pyridine, bipyridine, pyridazine, pyrimidine, bipyridamine, pyrazine, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, pyrrole, 2H-pyrrole, 3H-pyrrole, pyrazole, 2H-imidazole, 1,2,3-triazole, 1,2,4-triazole, indole, 3H-indole, 1H-isoindole, cyclopenta(b)pyridine, indazole, quinoline, bisquinoline, isoquinoline, bisisoquinoline, cinnoline, quinazoline, naphthyridine, piperidine, piperazine, pyrrolidine, pyrazolidine, quinuclidine, imidazolidine, picolylimine, purine, benzimidazole, bisimidazole, phenazine, acridine, and carbazole.
Examples of sulfur-containing heterocycles appropriate for L²and L³include thiophene, 1,2-dithiole, 1,3-dithiole, thiepin, benzo(b)thiophene, benzo(c)thiophene, thionaphthene, dibenzothiophene, 2H-thiopyran, 4H-thiopyran, and thioanthrene.
Examples of oxygen-containing heterocycles appropriate for L²and L³include 2H-pyran, 4H-pyran, 2-pyrone, 4-pyrone, 1,2-dioxin, 1,3-dioxin, oxepin, furan, 2H-1-benzopyran, coumarin, coumarone, chromene, chroman-4-one, isochromen-1-one, isochromen-3-one, xanthene, tetrahydrofuran, 1,4-dioxan, and dibenzofuran.
Examples of mixed heterocycles appropriate for L²and L³include isoxazole, oxazole, thiazole, isothiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,3,4-oxatriazole, 1,2,3,5-oxatriazole, 3H-1,2,3-dioxazole, 3H-1,2-oxathiole, 1,3-oxathiole, 4H-1,2-oxazine, 2H-1,3-oxazine, 1,4-oxazine, 1,2,5-oxathiazine, o-isooxazine, phenoxazine, phenothiazine, pyrano[3,4-b]pyrrole, indoxazine, benzoxazole, anthranil, and morpholine.
Preferred L²and L³ligands are aromatic nitrogen-containing and oxygen-containing heterocycles, and particularly preferred L²and L³ligands are monocyclic N-heteroaryl ligands that are optionally substituted with 1 to 3, preferably 1 or 2, substituents. Specific examples of particularly preferred L²and L³ligands are pyridine and substituted pyridines, such as 3-bromopyridine, 4-bromopyridine, 3,5-dibromopyridine, 2,4,6-tribromopyridine, 2,6-dibromopyridine, 3-chloropyridine, 4-chloropyridine, 3,5-dichloropyridine, 2,4,6-trichloropyridine, 2,6-dichloropyridine, 4-iodopyridine, 3,5-diiodopyridine, 3,5-dibromo-4-methylpyridine, 3,5-dichloro-4-methylpyridine, 3,5-dimethyl-4-bromopyridine, 3,5-dimethylpyridine, 4-methylpyridine, 3,5-diisopropylpyridine, 2,4,6-trimethylpyridine, 2,4,6-triisopropylpyridine, 4-(tert-butyl)pyridine, 4-phenylpyridine, 3,5-diphenylpyridine, 3,5-dichloro-4-phenylpyridine, and the like.
In general, any substituents present on L²and/or L³are selected from halo, C₁-C₂₀alkyl, substituted C₁-C₂₀alkyl, C₁-C₂₀heteroalkyl, substituted C₁-C₂₀heteroalkyl, C₅-C₂₄aryl, substituted C₅-C₂₄aryl, C₅-C₂₄heteroaryl, substituted C₅-C₂₄heteroaryl, C₆-C₂₄alkaryl, substituted C₆-C₂₄alkaryl, C₆-C₂₄heteroalkaryl, substituted C₆-C₂₄heteroalkaryl, C₆-C₂₄aralkyl, substituted C₆-C₂₄aralkyl, C₆-C₂₄heteroaralkyl, substituted C₆-C₂₄heteroaralkyl, and functional groups, with suitable functional groups including, without limitation, C₁-C₂₀alkoxy, C₅-C₂₄aryloxy, C₂-C₂₀alkylcarbonyl, C₆-C₂₄arylcarbonyl, C₂-C₂₀alkylcarbonyloxy, C₆-C₂₄arylcarbonyloxy, C₂-C₂₀alkoxycarbonyl, C₆-C₂₄aryloxycarbonyl, halocarbonyl, C₂-C₂₀alkylcarbonato, C₆-C₂₄arylcarbonato, carboxy, carboxylato, carbamoyl, mono-(C₁-C₂₀alkyl)-substituted carbamoyl, di-(C₁-C₂₀alkyl)-substituted carbamoyl, di-N—(C₁-C₂₀alkyl), N—(C₅-C₂₄aryl)-substituted carbamoyl, mono-(C₅-C₂₄aryl)-substituted carbamoyl, di-(C₆-C₂₄aryl)-substituted carbamoyl, thiocarbamoyl, mono-(C₁-C₂₀alkyl)-substituted thiocarbamoyl, di-(C₁-C₂₀alkyl)-substituted thiocarbamoyl, di-N—(C₁-C₂₀alkyl)-N—(C₆-C₂₄aryl)-substituted thiocarbamoyl, mono-(C₆-C₂₄aryl)-substituted thiocarbamoyl, di-(C₆-C₂₄aryl)-substituted thiocarbamoyl, carbamido, formyl, thioformyl, amino, mono-(C₁-C₂₀alkyl)-substituted amino, di-(C₁-C₂₀alkyl)-substituted amino, mono-(C₅-C₂₄aryl)-substituted amino, di-(C₅-C₂₄aryl)-substituted amino, di-N—(C₁-C₂₀alkyl),N—(C₅-C₂₄aryl)-substituted amino, C₂-C₂₀alkylamido, C₆-C₂₄arylamido, imino, C₁-C₂₀alkylimino, C₅-C₂₄arylimino, nitro, and nitroso. In addition, two adjacent substituents may be taken together to form a ring, generally a five- or six-membered alicyclic or aryl ring, optionally containing 1 to 3 heteroatoms and 1 to 3 substituents as above.
Preferred substituents on L²and L³include, without limitation, halo, C₁-C₁₂alkyl, substituted C₁-C₁₂alkyl, C₁-C₁₂heteroalkyl, substituted C₁-C₁₂heteroalkyl, C₅-C₁₄aryl, substituted C₅-C₁₄aryl, C₅-C₁₄heteroaryl, substituted C₅-C₁₄heteroaryl, C₆-C₁₆alkaryl, substituted C₆-C₁₆alkaryl, C₆-C₁₆heteroalkaryl, substituted C₆-C₁₆heteroalkaryl, C₆-C₁₆aralkyl, substituted C₆-C₁₆aralkyl, C₆-C₁₆heteroaralkyl, substituted C₆-C₁₆heteroaralkyl, C₁-C₁₂alkoxy, C₅-C₁₄aryloxy, C₂-C₁₂alkylcarbonyl, C₆-C₁₄arylcarbonyl, C₂-C₁₂alkylcarbonyloxy, C₆-C₁₄arylcarbonyloxy, C₂-C₁₂alkoxycarbonyl, C₆-C₁₄aryloxycarbonyl, halocarbonyl, formyl, amino, mono-(C₁-C₁₂alkyl)-substituted amino, di-(C₁-C₁₂alkyl)-substituted amino, mono-(C₅-C₁₄aryl)-substituted amino, di-(C₅-C₁₄aryl)-substituted amino, and nitro.
Of the foregoing, the most preferred substituents are halo, C₁-C₆alkyl, C₁-C₆haloalkyl, C₁-C₆alkoxy, phenyl, substituted phenyl, formyl, N,N-diC₁-C₆alkyl)amino, nitro, and nitrogen heterocycles as described above (including, for example, pyrrolidine, piperidine, piperazine, pyrazine, pyrimidine, pyridine, pyridazine, etc.).
L²and L³may also be taken together to form a bidentate or multidentate ligand containing two or more, generally two, coordinating heteroatoms such as N, O, S, or P, with preferred such ligands being diimine ligands of the Brookhart type. One representative bidentate ligand has the structure of formula (VIII)
wherein R¹⁵, R¹⁶, R¹⁷, and R¹⁸hydrocarbyl (e.g., C₁-C₂₀alkyl, C₂-C₂₀alkenyl, C₂-C₂₀alkynyl, C₅-C₂₄aryl, C₆-C₂₄alkaryl, or C₆-C₂₄aralkyl), substituted hydrocarbyl (e.g., substituted C₁-C₂₀alkyl, C₂-C₂₀alkenyl, C₂-C₂₀alkynyl, C₅-C₂₄aryl, C₆-C₂₄alkaryl, or C₆-C₂₄aralkyl), heteroatom-containing hydrocarbyl (e.g., C₁-C₂₀heteroalkyl, C₅-C₂₄heteroaryl, heteroatom-containing C₆-C₂₄aralkyl, or heteroatom-containing C₆-C₂₄alkaryl), or substituted heteroatom-containing hydrocarbyl (e.g., substituted C₁-C₂₀heteroalkyl, C₅-C₂₄heteroaryl, heteroatom-containing C₆-C₂₄aralkyl, or heteroatom-containing C₆-C₂₄alkaryl), or (1) R¹⁵and R¹⁶, (2) R¹⁷and R¹⁸, (3) R¹⁶and R¹⁷, or (4) both R¹⁵and R¹⁶, and R¹⁷and R¹⁸, may be taken together to form a ring, i.e., an N-heterocycle. Preferred cyclic groups in such a case are five- and six-membered rings, typically aromatic rings.
In a fourth group of catalysts that have the structure of formula (III), two of the substituents are taken together to form a bidentate ligand or a tridentate ligand. Examples of bidentate ligands include, but are not limited to, bisphosphines, dialkoxides, alkyldiketonates, and aryldiketonates. Specific examples include —P(Ph)₂CH₂CH₂P(Ph)₂-, —As(Ph)₂CH₂CH₂As(Ph₂)-, —P(Ph)₂CH₂CH₂C(CF₃)₂O—, binaphtholate dianions, pinacolate dianions, —P(CH₃)₂(CH₂)₂P(CH₃)₂—, and —OC(CH₃)₂(CH₃)₂CO—. Preferred bidentate ligands are —P(Ph)₂CH₂CH₂P(Ph)₂- and —P(CH₃)₂(CH₂)₂P(CH₃)₂—. Tridentate ligands include, but are not limited to, (CH₃)₂NCH₂CH₂P(Ph)CH₂CH₂N(CH₃)₂. Other preferred tridentate ligands are those in which any three of X¹, X², L¹, L², L³, R¹, and R²(e.g., X¹, L¹, and L²) are taken together to be cyclopentadienyl, indenyl, or fluorenyl, each optionally substituted with C₂-C₂₀alkenyl, C₂-C₂₀alkynyl, C₁-C₂₀alkyl, C₅-C₂₀aryl, C₁-C₂₀alkoxy, C₂-C₂₀alkenyloxy, C₂-C₂₀alkynyloxy, C₅-C₂₀aryloxy, C₂-C₂₀alkoxycarbonyl, C₁-C₂₀alkylthio, C₁-C₂₀alkylsulfonyl, or C₁-C₂₀alkylsulfinyl, each of which may be further substituted with C₁-C₆alkyl, halide, C₁-C₆alkoxy or with a phenyl group optionally substituted with halide, C₁-C₆alkyl, or C₁-C₆alkoxy. More preferably, in compounds of this type, X, L¹, and L²are taken together to be cyclopentadienyl or indenyl, each optionally substituted with vinyl, C₁-C₁₀alkyl, C₅-C₂₀aryl, C₁-C₁₀carboxylate, C₂-C₁₀alkoxycarbonyl, C₁-C₁₀alkoxy, or C₅-C₂₀aryloxy, each optionally substituted with C₁-C₆alkyl, halide, C₁-C₆alkoxy or with a phenyl group optionally substituted with halide, C₁-C₆alkyl or C₁-C₆alkoxy. Most preferably, X, L¹and L²may be taken together to be cyclopentadienyl, optionally substituted with vinyl, hydrogen, methyl, or phenyl. Tetradentate ligands include, but are not limited to O₂C(CH₂)₂P(Ph)(CH₂)₂P(Ph)(CH₂)₂CO₂, phthalocyanines, and porphyrins.
Complexes wherein L²and R²are linked are examples of the fourth group of catalysts, and are commonly called “Grubbs-Hoveyda” catalysts. Examples of Grubbs-Hoveyda-type catalysts include the following:
wherein L¹, X¹, X², and M are as described for any of the other groups of catalysts.
In addition to the catalysts that have the structure of formula (III), as described above, other transition metal carbene complexes include, but are not limited to:
neutral ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 16, are penta-coordinated, and are of the general formula (IX);
neutral ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 18, are hexa-coordinated, and are of the general formula (X);
cationic ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 14, are tetra-coordinated, and are of the general formula (XI); and
cationic ruthenium or osmium metal carbene complexes containing metal centers that are formally in the +2 oxidation state, have an electron count of 14, are tetra-coordinated, and are of the general formula (XII)
wherein:
X¹, X², L¹, L², n, L³, R¹, and R²are as defined for any of the previously defined four groups of catalysts; r and s are independently zero or 1; t is an integer in the range of zero to 5;
Y is any non-coordinating anion (e.g., a halide ion, BF₄ ⁻, etc.); Z¹and Z²are independently selected from —O—, —S—, —NR²—, —PR²—, —P(═O)R²—, —P(OR²)—, —P(═O)(OR²)—, —C(═O)—, —C(═O)O—, —OC(═O)—, —OC(═O)O—, —S(═O)—, and —S(═O)₂—; Z³is any cationic moiety such as —P(R²)₃ ⁺ or —N(R²)₃ ⁺; and
any two or more of X¹, X², L¹, L², L³, n, Z¹, Z², Z³, R¹, and R²may be taken together to form a cyclic group, e.g., a multidentate ligand, and
wherein any one or more of X¹, X², L¹, L², n, L³, Z¹, Z², Z³, R¹, and R²may be attached to a support.
Other suitable complexes include Group 8 transition metal carbenes bearing a cationic substituent, such as are disclosed in U.S. Pat. No. 7,365,140 (Piers et al.) having the general structure (XIII):
wherein:
M is a Group 8 transition metal;
L¹and L²are neutral electron donor ligands;
X¹and X²are anionic ligands;
R¹is hydrogen, C₁-C₁₂hydrocarbyl, or substituted C₁-C₁₂hydrocarbyl;
W is an optionally substituted and/or heteroatom-containing C₁-C₂₀hydrocarbylene linkage;
Y is a positively charged Group 15 or Group 16 element substituted with hydrogen, C₁-C₁₂hydrocarbyl, substituted C₁-C₁₂hydrocarbyl; heteroatom-containing C₁-C₁₂hydrocarbyl, or substituted heteroatom-containing hydrocarbyl;
Z⁻ is a negatively charged counterion;
m is zero or 1; and
n is zero or 1;

- wherein any two or more of L¹, L², X¹, X², R¹, W, and Y can be taken together to form a cyclic group.
- Each of M, L¹, L², X¹, and X²in structure (XIII) may be as previously defined herein.

W is an optionally substituted and/or heteroatom-containing C₁-C₂₀hydrocarbylene linkage, typically an optionally substituted C₁-C₁₂alkylene linkage, e.g., —(CH₂)_i— where i is an integer in the range of 1 to 12 inclusive and any of the hydrogen atoms may be replaced with a non-hydrogen substituent as described earlier herein with regard to the definition of the term “substituted.” The subscript n is zero or 1, meaning that W may or may not be present. In a preferred embodiment, n is zero.
Y is a positively charged Group 15 or Group 16 element substituted with hydrogen, C₁-C₁₂hydrocarbyl, substituted C₁-C₁₂hydrocarbyl, heteroatom-containing C₁-C₁₂hydrocarbyl, or substituted heteroatom-containing hydrocarbyl. Preferably, Y is a C₁-C₁₂hydrocarbyl-substituted, positively charged Group 15 or Group 16 element. Representative Y groups include P(R²)₃, P(R²)₃, As(R²)₃, S(R²)₂, O(R²)₂, where the R²are independently selected from C₁-C₁₂hydrocarbyl; within these, preferred Y groups are phosphines of the structure P(R²)₃wherein the R²are independently selected from C₁-C₁₂alkyl and aryl, and thus include, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, cyclopentyl, cyclohexyl, and phenyl. Y can also be a heterocyclic group containing the positively charged Group 15 or Group 16 element. For instance, when the Group 15 or Group 16 element is nitrogen, Y may be an optionally substituted pyridinyl, pyrazinyl, or imidazolyl group.
Z⁻ is a negatively charged counterion associated with the cationic complex, and may be virtually any anion, so long as the anion is inert with respect to the components of the complex and the reactants and reagents used in the metathesis reaction catalyzed. Preferred Z⁻ moieties are weakly coordinating anions, such as, for instance, [B(C₆F₅)₄]⁻, [BF₄]⁻, [B(C₆H₆)₄]⁻, [CF₃S(O)₃]⁻, [PF₆]⁻, [SbF₆]⁻, [AlCl₄]⁻, [FSO₃]⁻, [CB₁₁H₆Cl₆]⁻, [CB₁₁H₆Br₆]⁻, and [SO₃F:SbF₅]⁻. Preferred anions suitable as Z⁻ are of the formula B(R¹⁵)₄ ⁻ where R¹⁵is fluoro, aryl, or perfluorinated aryl, typically fluoro or perfluorinated aryl. Most preferred anions suitable as Z⁻ are BF₄ ⁻ and B(C₆F₅)⁻, optimally the latter.
It should be emphasized that any two or more of X¹, X², L¹, L², R¹, W, and Y can be taken together to form a cyclic group, as disclosed, for example, in U.S. Pat. No. 5,312,940 to Grubbs et al. When any of X¹, X², L¹, L², R¹, W, and Y are linked to form cyclic groups, those cyclic groups may be five- or six-membered rings, or may comprise two or three five- or six-membered rings, which may be either fused or linked. The cyclic groups may be aliphatic or aromatic, and may be heteroatom-containing and/or substituted, as explained in part (I) of this section.
One group of exemplary catalysts encompassed by the structure of formula (XIII) are those wherein m and n are zero, such that the complex has the structure of formula (XIV)
Possible and preferred X¹, X², and L¹ligands are as described earlier with respect to complexes of formula (I), as are possible and preferred Y⁺ and Z⁻ moieties. M is Ru or Os, preferably Ru, and R¹is hydrogen or C₁-C₁₂alkyl, preferably hydrogen.
In formula (XIV)-type catalysts, L¹is preferably a heteroatom-containing carbene ligand having the structure of formula (XV)
such that complex (XIV) has the structure of formula (XVI)
wherein X¹, X², R¹, R², Y, and Z are as defined previously, and the remaining substituents are as follows:
Z¹and Z²are heteroatoms typically selected from N, O, S, and P. Since O and S are divalent, j is necessarily zero when Z¹is O or S, and k is necessarily zero when Z²is O or S. However, when Z¹is N or P, then j is 1, and when Z²is N or P, then k is 1. In a preferred embodiment, both Z¹and Z²are N.
Q¹, Q², Q³, and Q⁴are linkers, e.g., C₁-C₁₂hydrocarbylene, substituted C₁-C₁₂hydrocarbylene, heteroatom-containing C₁-C₁₂hydrocarbylene, substituted heteroatom-containing C₁-C₁₂hydrocarbylene, or —(CO)—, and w, x, y, and z are independently zero or 1, meaning that each linker is optional. Preferably, w, x, y, and z are all zero.
R³, R^3A, R⁴, and R^4Aare independently selected from hydrogen, hydrogen, C₁-C₂₀hydrocarbyl, substituted C₁-C₂₀hydrocarbyl, heteroatom-containing C₁-C₂₀hydrocarbyl, and substituted heteroatom-containing C₁-C₂₀hydrocarbyl.
Preferably, w, x, y, and z are zero, Z¹and Z¹are N, and R^3Aand R^4Aare linked to form -Q-, such that the complex has the structure of formula (XVII)
wherein R³and R⁴are defined above, with preferably at least one of R³and R⁴, and more preferably both R³and R⁴, being alicyclic or aromatic of one to about five rings, and optionally containing one or more heteroatoms and/or substituents. Q is a linker, typically a hydrocarbylene linker, including C₁-C₁₂hydrocarbylene, substituted C₁-C₁₂hydrocarbylene, heteroatom-containing C₁-C₁₂hydrocarbylene, or substituted heteroatom-containing C₁-C₁₂hydrocarbylene linker, wherein two or more substituents on adjacent atoms within Q may be linked to form an additional cyclic structure, which may be similarly substituted to provide a fused polycyclic structure of two to about five cyclic groups. Q is often, although not necessarily, a two-atom linkage or a three-atom linkage, e.g., —CH₂—CH₂—, —CH(Ph)-CH(Ph)-where Ph is phenyl; ═CR—N═, giving rise to an unsubstituted (when R═H) or substituted (R=other than H) triazolyl group; or —CH₂—SiR₂—CH₂— (where R is H, alkyl, alkoxy, etc.).
In a more preferred embodiment, Q is a two-atom linkage having the structure —CR⁸R⁹—CR¹⁰R¹¹— or —CR⁸═CR¹⁰—, preferably —CR⁸R⁹—CR¹⁰R¹¹—, wherein R⁸, R⁹, R¹⁰, and R¹¹are independently selected from hydrogen, C₁-C₁₂hydrocarbyl, substituted C₁-C₁₂hydrocarbyl, heteroatom-containing C₁-C₁₂hydrocarbyl, substituted heteroatom-containing C₁-C₁₂hydrocarbyl, and functional groups as defined in part (I) of this section. Examples of functional groups here include carboxyl, C₁-C₂₀alkoxy, C₅-C₂₀aryloxy, C₂-C₂₀alkoxycarbonyl, C₂-C₂₀alkoxycarbonyl, C₂-C₂₀acyloxy, C₁-C₂₀alkylthio, C₅-C₂₀arylthio, C₁-C₂₀alkylsulfonyl, and C₁-C₂₀alkylsulfinyl, optionally substituted with one or more moieties selected from C₁-C₁₀alkyl, C₁-C₁₀alkoxy, C₅-C₂₀aryl, hydroxyl, sulfhydryl, formyl, and halide. Alternatively, any two of R⁸, R⁹, R¹⁰, and R¹¹m may be linked together to form a substituted or unsubstituted, saturated or unsaturated ring structure, e.g., a C₄-C₁₂alicyclic group or a C₅or C₆aryl group, which may itself be substituted, e.g., with linked or fused alicyclic or aromatic groups, or with other substituents.
Further details concerning such formula (XIII) complexes, as well as associated preparation methods, may be obtained from U.S. Pat. No. 7,365,140, herein incorporated by reference.
As is understood in the field of catalysis, suitable solid supports for any of the catalysts described herein may be of synthetic, semi-synthetic, or naturally occurring materials, which may be organic or inorganic, e.g., polymeric, ceramic, or metallic. Attachment to the support will generally, although not necessarily, be covalent, and the covalent linkage may be direct or indirect, if indirect, typically through a functional group on a support surface.
Non-limiting examples that may be used in the reactions of the disclosure include the following, some of which for convenience are identified throughout this disclosure by reference to their molecular weight:
In the foregoing molecular structures and formulae, Ph represents phenyl, Cy represents cyclohexane, Me represents methyl, nBu represents n-butyl, i-Pr represents isopropyl, py represents pyridine (coordinated through the N atom), and Mes represents mesityl (i.e., 2,4,6-trimethylphenyl).
Further examples of catalysts useful in the reactions of the present disclosure include the following: ruthenium (II) dichloro(3-methyl-1,2-butenylidene)bis(tricyclopentylphosphine) (C716); ruthenium (II) dichloro(3-methyl-1,2-butenylidene)bis(tricyclohexylphosphine) (C801); ruthenium (II) dichloro(phenylmethylene)bis(tricyclohexylphosphine) (C823); ruthenium (II) [1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(triphenylphosphine) (C830), and ruthenium (II) dichloro(vinyl phenylmethylene)bis(tricyclohexylphosphine) (C835); ruthenium (II) dichloro (tricyclohexylphosphine) (o-isopropoxyphenylmethylene) (C601), and ruthenium (II) (1,3-bis-(2,4,6,-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene) (bis 3-bromopyridine (C884)).
Exemplary ruthenium-based metathesis catalysts include those represented by structures 12 (commonly known as Grubbs's catalyst), 14 and 16. Structures 18, 20, 22, 24, 26, 28, 60, 62, 64, 66, and 68 represent additional ruthenium-based metathesis catalysts. Catalysts C627, C682, C697, C712, and C827 represent still additional ruthenium-based catalysts. General structures 50 and 52 represent additional ruthenium-based metathesis catalysts of the type reported in Chemical & Engineering News; Feb. 12, 2007, at pages 37-47. In the structures, Ph is phenyl, Mes is mesityl, py is pyridine, Cp is cyclopentyl, and Cy is cyclohexyl.
Techniques for using the metathesis catalysts are known in the art (see, for example, U.S. Pat. Nos. 7,102,047; 6,794,534; 6,696,597; 6,414,097; 6,306,988; 5,922,863; 5,750,815; and metathesis catalysts with ligands in U.S. Publication No. 2007/0004917 A1), all incorporated by reference herein in their entireties. A number of the metathesis catalysts as shown are manufactured by Materia, Inc. (Pasadena, Calif.).
Additional exemplary metathesis catalysts include, without limitation, metal carbene complexes selected from the group consisting of molybdenum, osmium, chromium, rhenium, and tungsten. The term “complex” refers to a metal atom, such as a transition metal atom, with at least one ligand or complexing agent coordinated or bound thereto. Such a ligand typically is a Lewis base in metal carbene complexes useful for alkyne or alkene-metathesis. Typical examples of such ligands include phosphines, halides and stabilized carbenes. Some metathesis catalysts may employ plural metals or metal co-catalysts (e.g., a catalyst comprising a tungsten halide, a tetraalkyl tin compound, and an organoaluminum compound).
An immobilized catalyst can be used for the metathesis process. An immobilized catalyst is a system comprising a catalyst and a support, the catalyst associated with the support. Exemplary associations between the catalyst and the support may occur by way of chemical bonds or weak interactions (e.g. hydrogen bonds, donor acceptor interactions) between the catalyst, or any portions thereof, and the support or any portions thereof. Support is intended to include any material suitable to support the catalyst. Typically, immobilized catalysts are solid phase catalysts that act on liquid or gas phase reactants and products. Exemplary supports are polymers, silica or alumina. Such an immobilized catalyst may be used in a flow process. An immobilized catalyst can simplify purification of products and recovery of the catalyst so that recycling the catalyst may be more convenient.
The metathesis process can be conducted under any conditions adequate to produce the desired metathesis products. For example, stoichiometry, atmosphere, solvent, temperature and pressure can be selected to produce a desired product and to minimize undesirable byproducts. The metathesis process may be conducted under an inert atmosphere. Similarly, if a reagent is supplied as a gas, an inert gaseous diluent can be used. The inert atmosphere or inert gaseous diluent typically is an inert gas, meaning that the gas does not interact with the metathesis catalyst to substantially impede catalysis. For example, particular inert gases are selected from the group consisting of helium, neon, argon, nitrogen and combinations thereof.
Similarly, if a solvent is used, the solvent chosen may be selected to be substantially inert with respect to the metathesis catalyst. For example, substantially inert solvents include, without limitation, aromatic hydrocarbons, such as benzene, toluene, xylenes, etc.; halogenated aromatic hydrocarbons, such as chlorobenzene and dichlorobenzene; aliphatic solvents, including pentane, hexane, heptane, cyclohexane, etc.; and chlorinated alkanes, such as dichloromethane, chloroform, dichloroethane, etc.
In certain embodiments, a ligand may be added to the metathesis reaction mixture. In many embodiments using a ligand, the ligand is selected to be a molecule that stabilizes the catalyst, and may thus provide an increased turnover number for the catalyst. In some cases the ligand can alter reaction selectivity and product distribution. Examples of ligands that can be used include Lewis base ligands, such as, without limitation, trialkylphosphines, for example tricyclohexylphosphine and tributyl phosphine; triarylphosphines, such as triphenylphosphine; diarylalkylphosphines, such as, diphenylcyclohexylphosphine; pyridines, such as 2,6-dimethylpyridine, 2,4,6-trimethylpyridine; as well as other Lewis basic ligands, such as phosphine oxides and phosphinites. Additives may also be present during metathesis that increase catalyst lifetime.
Any useful amount of the selected metathesis catalyst can be used in the process. For example, the molar ratio of the unsaturated polyol ester to catalyst may range from about 5:1 to about 10,000,000:1 or from about 50:1 to 500,000:1.
The metathesis reaction temperature may be a rate-controlling variable where the temperature is selected to provide a desired product at an acceptable rate. The metathesis temperature may be greater than −40° C., may be greater than about −20° C., and is typically greater than about 0° C. or greater than about 20° C. Typically, the metathesis reaction temperature is less than about 150° C., typically less than about 120° C. An exemplary temperature range for the metathesis reaction ranges from about 20° C. to about 120° C.
The metathesis reaction can be run under any desired pressure. Typically, it will be desirable to maintain a total pressure that is high enough to keep the cross-metathesis reagent in solution. Therefore, as the molecular weight of the cross-metathesis reagent increases, the lower pressure range typically decreases since the boiling point of the cross-metathesis reagent increases. The total pressure may be selected to be greater than about 10 kPa, in some embodiments greater than about 30 kP, or greater than about 100 kPa. Typically, the reaction pressure is no more than about 7000 kPa, in some embodiments no more than about 3000 kPa. An exemplary pressure range for the metathesis reaction is from about 100 kPa to about 3000 kPa.
In some embodiments, the metathesis reaction is catalyzed by a system containing both a transition and a non-transition metal component. The most active and largest number of catalyst systems are derived from Group VI A transition metals, for example, tungsten and molybdenum.

Separation Step (Step (c)):

After cross-metathesis with the short-chain olefin, at least a portion of the acid-, ester-, or salt-functionalized alkene is separated from the remaining cross-metathesis products. Useful techniques for separating the acid-, ester-, or salt-functionalized alkene include, for example, distillation, reactive distillation, chromatography, fractional crystallization, membrane separation, liquid/liquid extraction, or a combination thereof.

Catalytic Modification (Step (d)):

According to the method of the invention, after separation, the carbon-carbon double bond of the separated acid-, ester-, or carboxylate salt-functionalized alkene is catalytically modified by hydrocyanation in order to introduce a nitrile group into the molecule. In some embodiments, the nitrile group is then further reacted to form an amine group, a carboxylic acid group, an aldehyde group, or an alcohol group.
Hydrocyanation is a catalytic process where hydrogen cyanide is added to an alkene having n carbon atoms, to produce a nitrile having n+1 carbon atoms, with n≧1. In many embodiments, prior to hydrocyanation, the internal functionalized alkene is isomerized to form a terminal functionalized alkene. Isomerization and hydrocyanation of an exemplary acid-, ester-, or salt-functionalized compound is shown below:
R′OOC—(CH₂)_n—CH═CH—CH₃
R′OOC—(CH₂)_n—CH₂—CH═CH₂
R′OOC—(CH₂)_n—CH₂—CH═CH₂+HCN/catalyst→R′OOC—(CH₂)_n—CH₂—CH(—C≡N)—CH₃+R′OOC—(CH₂)_n—CH₂—CH₂—CH₂—C≡N
where —R′ is hydrogen (acid), an aliphatic group (ester), or a metal ion (salt).
As shown above, hydrocyanation may result in the formation of branched or linear species depending upon the location of the carbon-carbon double bond and whether isomerization of the double bond occurs before the hydrocyanation reaction. Typical hydrocyanation catalysts include low valent nickel phosphite catalysts. Optionally, the nitrile group may be hydrogenated to convert it into a primary amine group as shown below:
R′OOC—(CH₂)_n—CH₂—CH(C≡N)—CH₃+H₂/catalyst→R′OOC—(CH₂)_n—CH₂—CH(—CH₂—NH₂)—CH₃
R′OOC—(CH₂)_n—CH₂—CH₂—CH₂—C≡N+H₂/catalyst→R′OOC—(CH₂)_n—CH₂—CH₂—CH₂—CH₂—NH₂
where —R′ is hydrogen (acid), an aliphatic group (ester), or a metal ion (salt). Examples of hydrogenation catalysts include Ru, Pt, Pd, Rh, and Re catalysts.
The method of the invention can be employed to synthesize various organic compounds. The organic compounds produced in accordance with the method of the present invention will depend upon the starting composition that is chosen and the catalytic modification. For example, an ester-functionalized starting composition can be catalytically modified using hydrocyanation to produce an ester-nitrile compound. In similar fashion, an acid-functionalized starting composition can be catalytically modified by hydrocyanation to produce an organic compound having carboxylic acid functionality and nitrile functionality. The nitrile group may also be modified to an aldehyde, alcohol, carboxylic acid, or amine group. Additional examples are summarized in TABLE C.

TABLE C

Functionality of		Functionality of
Starting	Catalytic	Product Organic
Composition	Modification	Compound

Acid	Hydrocyanation &	Acid - Amine
	Hydrogenation
Acid	Hydrocyanation &	Diacid
	Hydrolysis
Acid	Hydrocyanation &	Acid - Aldehyde
	Reduction
Acid	Hydrocyanation &	Acid - Alcohol
	Reduction
Ester	Hydrocyanation &	Ester - Amine
	Hydrogenation
Ester	Hydrocyanation &	Ester - Acid
	Hydrolysis
Ester	Hydrocyanation &	Ester - Aldehyde
	Reduction
Ester	Hydrocyanation &	Ester - Alcohol
	Reduction

The length of the product organic made in accordance with the method of the invention can be varied depending upon the starting composition that is chosen and the position of the carbon-carbon double bond in the starting composition. Typically, the organic compounds will have a chain length of about 8 to 16 carbon atoms. For example, when Δ9 starting compositions are used, the method of the invention produces organic compounds having a chain length of 12 carbon atoms (C12) when 3-hexene is used as the short chain alkene in the cross-metathesis reaction. A summary of the starting composition and the chain length of the resulting organic compound is provided in TABLE D.

	TABLE D

		Chain Length of
	Starting	Organic
	Composition	Compound

	Δ4	7
	Δ5	8
	Δ6	9
	Δ8	11
	Δ9	12
	Δ11	14
	Δ13	16

Using the method of the invention it is possible to synthesize a large number of organic compounds having a variety of chain lengths and functional groups. A summary of some organic compounds that can be synthesized using the method of the invention is provided in TABLE E.

TABLE E

	Cross-	Functionalized
Starting	Metathesis	Alkene	Catalytic
Composition	Reagent	Intermediate	Modification	Products

Δ9 methyl	2-butene	Methyl ester of 9-	Hydrocyanation &	Methyl 12-
ester		undecenoic acid	Hydrogenation	aminododecanoate
				H₂N(CH₂)₁₁CO₂CH₃
Δ9 methyl	2-butene	Methyl ester of 9-	Hydrocyanation &	Methyl 11-
ester		undecenoic acid	Hydrolysis	carboxyundecanoate
				HOOC(CH₂)₁₀CO₂CH₃
Δ9 methyl	2-butene	Methyl ester of 9-	Hydrocyanation &	Methyl 12-
ester		undecenoic acid	Reduction	oxododecanoate
				OHC(CH₂)₁₀CO₂CH₃
Δ9 methyl	2-butene	Methyl ester of 9-	Hydrocyanation &	Methyl 12-
ester		undecenoic acid	Reduction	hydroxydodecanoate
				HO(CH₂)₁₁CO₂CH₃
Δ9 acid	2-butene	9-undecenoic	Hydrocyanation &	12-Aminododecanoic acid
		acid	Hydrogenation	H₂N(CH₂)₁₁CO₂H
Δ9 acid	2-butene	9-undecenoic	Hydrocyanation &	1,12-Dodecanedioc acid
		acid	Hydrolysis	HOOC(CH₂)₁₀COOH
Δ9 acid	2-butene	9-undecenoic	Hydrocyanation &	12-oxododecanoic acid
		acid	Reduction	OHC(CH₂)₁₀CO₂H
Δ9 acid	2-butene	9-undecenoic	Hydrocyanation &	12-Hydroxydodecanoic
		acid	Reduction	acid
				HO(CH₂)₁₁CO₂H

Other embodiments of this invention will be apparent to those skilled in the art upon consideration of this specification or from practice of the invention disclosed herein. Various omissions, modifications, and changes to the principles and embodiments described herein may be made by one skilled in the art without departing from the true scope and spirit of the invention which is indicated by the following claims. All patents, patent documents, and publications cited herein are hereby incorporated by reference as if individually incorporated.

Claims

1-55. (canceled)

56. A method for making an organic compound, the method comprising:

(a) providing an unsaturated glyceride, wherein the unsaturated glyceride comprises up to three fatty acid moieties selected from the group consisting of monounsaturated fatty acids, polyunsaturated fatty acids, and saturated fatty acids, provided that the unsaturated glyceride comprises at least one unsaturated fatty acid moiety;

(b) reacting the unsaturated glyceride with a monohydric alcohol to form a monoester of the at least one unsaturated fatty acid of step (a);

(c) reacting the monoester of step (b) with an alpha olefin, an internal olefin, or a mixture thereof, in the presence of a metathesis catalyst to form a cross-metathesized unsaturated monoester; and

(d) hydrocyanating at least one carbon-carbon double bond of the cross-metathesized unsaturated monoester of step (c) to form a hydrocyanated monoester.

57. The method of claim 56, further comprising hydrogenating the hydrocyanated monoester to form an aminated monoester.

58. The method of claim 56, further comprising hydrolyzing the hydrocyanated monoester to form a hydrocyanated carboxylic acid.

59. The method of claim 56, further comprising reducing the hydrocyanated monoester to form a formylated monoester.

60. The method of claim 56, further comprising reducing the hydrocyanated monoester to form a hydroxylated monoester.

61. The method of claim 56, wherein the at least one unsaturated fatty acid moiety is a delta-9 fatty acid moiety.

62. The method of claim 61, wherein the at least one unsaturated fatty acid moiety is an oleic acid moiety, a linoleic acid moiety, or a linolenic acid moiety.

63. The method of claim 56, wherein the monohydric alcohol is selected from the group consisting of methanol, ethanol, propanol, isopropanol, and butanol.

64. The method of claim 63, wherein the monohydric alcohol is methanol.

65. The method of claim 56, wherein step (c) comprises reacting the monoester of step (b) with an alpha olefin.

66. The method of claim 65, wherein the alpha olefin is selected from the group consisting of: ethylene, 1-propene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, and 1-nonene.

67. The method of claim 56, wherein step (c) comprises reacting the monoester of step (b) with an internal olefin.

68. The method of claim 67, wherein the internal olefin is selected from the group consisting of: 2-butene, 3-hexene, 4-octene, 2-pentene, 2-hexene, 2-heptene, 3-heptene, 2-octene, 3-octene, 2-nonene, 3-nonene, and 4-nonene.

69. The method of claim 56, wherein the cross-metathesized unsaturated monoester is a monoester of 9-decenoid acid, 9-undecenoid acid, or 9-dodecenoic acid.

70. The method of claim 56, wherein the cross-metathesized unsaturated monoester is a monoester is an internally unsaturated monoester.

71. The method of claim 70, wherein the internally unsaturated monoester is a monoester of 9-undecenoid acid or 9-dodecenoic acid.

72. The method of claim 70, comprising isomerizing the internally unsaturated monoester to form a terminally unsaturated monoester.

73. The method of claim 71, comprising isomerizing the internally unsaturated monoester to form a monoester of 10-undecenoic acid or 11-dodecenoic acid.

74. The method of claim 56, wherein the unsaturated glyceride is derived from a natural oil.

75. The method of claim 74, wherein the natural oil comprises plant-based oils, animal fats, algae oils, or combinations thereof.