US2016185689A1PendingUtilityA1

Synthesis of terminal alkenes from internal alkenes and ethylene via olefin metathesis

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Assignee: MATERIA INCPriority: Jul 13, 2006Filed: Dec 31, 2015Published: Jun 30, 2016
Est. expiryJul 13, 2026(expired)· nominal 20-yr term from priority
Inventors:Yann Schrodi
C07C 6/04C07C 2531/18C07F 15/0046C07C 2531/28B01J 31/12C07C 2531/22C07C 67/333C07C 2531/24B01J 31/2265B01J 2231/543B01J 2531/821
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Claims

Abstract

This invention relates generally to olefin metathesis, and more particularly relates to the synthesis of terminal alkenes from internal alkenes using a cross-metathesis reaction catalyzed by a selected olefin metathesis catalyst. In one embodiment of the invention, for example, a method is provided for synthesizing a terminal olefin, the method comprising contacting an olefinic substrate comprised of at least one internal olefin with ethylene, in the presence of a metathesis catalyst, wherein the catalyst is present in an amount that is less than about 1000 ppm relative to the olefinic substrate, and wherein the metathesis catalyst has the structure of formula (II) wherein the various substituents are as defined herein. The invention has utility, for example, in the fields of catalysis, organic synthesis, and industrial chemistry.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for synthesizing a metathesis reaction product having a terminal olefin, the method comprising contacting, in the presence of a metathesis catalyst, an olefinic substrate comprised of at least one internal olefin with ethylene, wherein the catalyst is present in an amount that is less than about 1000 ppm relative to the amount of the olefinic substrate, and wherein the metathesis catalyst has the structure of formula (II): 
       
         
           
           
               
               
           
         
       
       wherein:
 M is Ru or Os; 
 m is zero, 1, or 2; 
 n1 and n2 are independently selected from zero and 1; 
 X 1  and X 2  are anionic ligands; 
 R 1  and R 2  are independently selected from the group consisting of hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl; 
 L 2  and L 3  are independently neutral electron donating ligands; 
 L 1  is a carbene ligand with the structure of formula (IIIb): 
 
       
         
           
           
               
               
           
         
       
       wherein Ar 1  is an aryl substituted with at least one group selected from the group consisting of C 2 -C 12  alkyl, C 2 -C 12  alkenyl, C 2 -C 12  alkynyl, C 5 -C 12  aryl, C 6 -C 12  aralkyl, and C 6 -C 12  alkaryl; a is an optional double bond; and R 10 , R 11 , R 13 , R 14 , R 15  and R 16  are independently selected from the group consisting of hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, and substituted heteroatom-containing hydrocarbyl, wherein any two or more of Ar 1 , R 10 , R 11 , R 13 , R 14 , R 15 , and R 16  may be taken together to form a cyclic group, and provided that R 14  and R 16  are not present if a is present. 
     
     
         2 . The method of  claim 1 , wherein Ar 1  has the structure of formula (VIIa): 
       
         
           
           
               
               
           
         
       
       wherein   represents the attachment point to N in formula (IIIb), R 17  and R 18  are independently selected from the group consisting of C 2 -C 12  alkyl, C 2 -C 12  alkenyl, C 2 -C 12  alkynyl, C 5 -C 12  aryl, C 6 -C 12  aralkyl, and C 6 -C 12  alkaryl, and R 19 , R 20 , and R 21  are independently selected from the group consisting of hydrogen, C 1 -C 12  alkyl, C 2 -C 12  alkenyl, C 2 -C 12  alkynyl, C 5 -C 12  aryl, C 6 -C 12  aralkyl, and C 6 -C 12  alkaryl. 
     
     
         3 . The method of  claim 2 , wherein R 19 , R 20 , and R 21  are hydrogen such that Ar 1  has the structure of formula (VIIb): 
       
         
           
           
               
               
           
         
       
     
     
         4 . The method of  claim 1 , wherein the olefinic substrate is selected from the group consisting of seed oils, alkyl esters of unsaturated fatty acids, and aryl esters of unsaturated fatty acids. 
     
     
         5 . The method of  claim 1 , wherein the olefinic substrate comprises a mixture of internal olefins selected from the group consisting of monoacylglycerols, diacylglycerols, triacylglycerols, and combinations thereof. 
     
     
         6 . The method of  claim 1 , wherein the olefinic substrate is of the formula (R I )(R II )C═C(R III )(R IV ), wherein R I , R II , R III , and R IV  are independently selected from the group consisting of hydrogen, hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, substituted heteroatom-containing hydrocarbyl, and functional groups, provided that at least one of R I  or R II  and at least one of R III  or R IV  is other than hydrogen.

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