Jump to main content
Jump to site search

Issue 20, 2016
Previous Article Next Article

Methyl vinyl glycolate as a diverse platform molecule

Author affiliations

Abstract

Methyl vinyl glycolate (methyl 2-hydroxybut-3-enoate, MVG) is available by zeolite catalyzed degradation of mono- and disaccharides and has the potential to become a renewable platform molecule for commercially relevant catalytic transformations. This is further illustrated here by the development of four reactions to afford industrially promising structures. Catalytic homo metathesis of MVG using Grubbs-type catalysts affords the crystalline dimer dimethyl (E)-2,5-dihydroxyhex-3-enedioate in excellent yield and with meso stereochemical configuration. Cross metathesis reactions between MVG and various long-chain terminal olefins give unsaturated α-hydroxy fatty acid methyl esters in good yields. [3,3]-Sigmatropic rearrangements of MVG also proceed in good yields to give unsaturated adipic acid derivatives. Finally, rearrangement of the allylic acetate of MVG proceeds in acceptable yield to afford methyl 4-acetoxycrotonate.

Graphical abstract: Methyl vinyl glycolate as a diverse platform molecule

Back to tab navigation

Supplementary files

Publication details

The article was received on 07 Jun 2016, accepted on 02 Aug 2016 and first published on 02 Aug 2016


Article type: Paper
DOI: 10.1039/C6GC01556E
Citation: Green Chem., 2016,18, 5448-5455
  •   Request permissions

    Methyl vinyl glycolate as a diverse platform molecule

    A. Sølvhøj, E. Taarning and R. Madsen, Green Chem., 2016, 18, 5448
    DOI: 10.1039/C6GC01556E

Search articles by author

Spotlight

Advertisements