New synthesis of 3-trifluoromethylpyrroles by condensation of mesoionic 4-trifluoroacetyl-1,3-oxazolium-5-olates with phosphorus ylides

Org Lett. 2010 Nov 5;12(21):4776-9. doi: 10.1021/ol1018689.

Abstract

Mesoionic 4-trifluoroacetyl-1,3-oxazolium-5-olates (1), obtained from the reaction of N-acyl-N-alkylglycines with trifluoroacetic anhydride, react with phosphorus ylides to give β-trifluoromethylpyrroles (2) in good yields. The novel ring transformations of 1 into 2 occur via an initial attack of the ylide anions on the C-2 position of the ring.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Fluorine Compounds / chemical synthesis*
  • Ions / chemistry
  • Methylation
  • Molecular Structure
  • Oxazoles / chemistry*
  • Phosphorus / chemistry*
  • Pyrroles / chemical synthesis*

Substances

  • Fluorine Compounds
  • Ions
  • Oxazoles
  • Pyrroles
  • Phosphorus