Challenging cyclopropanation reactions on non-activated double bonds of fatty esters. Issue 32 (31st March 2017)

• Record Type: Journal Article
• Authors: Angulo, B.; Fraile, J. M.; Herrerías, C. I.; Mayoral, J. A.
• Is Part Of: RSC advances. Volume 7:Issue 32(2017)
• Page Start: 19417
• Page End: 19424
• Publication Date: 2017-03-31
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c7ra01017f
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Cyclopropanation reactions in the chain of unsaturated fatty esters is a good strategy for the ready preparation of potential monomers for polymerization. Abstract : Monounsaturated fatty esters with non-activated double bonds have been made to react with two different diazocompounds, ethyl diazoacetate (EDA) and dimethyl diazomalonate (DDM), in copper and rhodium catalyzed cyclopropanation reactions. The corresponding cyclopropanes have been obtained with quantitative or nearly quantitative yields (>99%) in all the cases, with only the exception of the reaction of methyl elaidate, an E alkene, with the less reactive DDM. For the first time, the two stereoisomers of ethyl (2 R *, 3 S *)-2-(7-methoxycarbonyl)heptyl-3-octylcyclopropane-1-carboxylate, obtained from the reaction of methyl oleate and EDA, have been separated and fully characterized. Finally, the diesters and triesters with cyclopropane structure have been reduced to diols and triols, and hydrolyzed to the corresponding diacids and triacids, to demonstrate the potential usefulness of this methodology to prepare monomers from renewable sources.