Facile synthesis of (Z)-tetracos-5-enoic acid and racemic cis-4-(2-octadecylcyclopropane-1-yl)-butanoic acid

Chem Phys Lipids. 2003 Nov;126(1):49-53. doi: 10.1016/s0009-3084(03)00092-6.

Abstract

(Z)-tetracos-5-enoic acid and racemic cis-4-(2-octadecylcyclopropane-1-yl)-butanoic acid have been prepared from 1-eicosene by a new facile route. Periodic acid cleavage of the epoxide of 1-eicosene gave nonadecanal which was condensed with 4-carboxybutyltriphenylphosphonium bromide to give predominately (Z)-tetracos-5-enoic acid. Simmons-Smith type cyclopropanation of (Z)-tetracos-5-enoic acid gave a minor proportion of racemic cis-4-(2-octadecylcyclopropane-1-yl)-butanoic acid accompanied by major amounts of its methyl ester.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria / chemistry
  • Bacteria / ultrastructure
  • Butyrates / chemical synthesis*
  • Butyric Acid / chemical synthesis*
  • Cell Wall / chemistry
  • Fatty Acids, Monounsaturated / chemical synthesis*
  • Stereoisomerism

Substances

  • 4-(2-octadecylcyclopropane-1-yl)butanoic acid
  • Butyrates
  • Fatty Acids, Monounsaturated
  • Butyric Acid
  • tetracosenoic acid