Palladium-catalyzed direct ortho-acylation through an oxidative coupling of acetanilides with toluene derivatives

J Org Chem. 2012 Dec 21;77(24):11339-44. doi: 10.1021/jo302125h. Epub 2012 Nov 30.

Abstract

A facile ortho-acylation of acetanilides by a Pd-catalyzed oxidative C-H activation was developed in which low toxic, stable, and commercially available toluene derivatives were first used as acylation reagents by a tandem reaction to form o-acylacetanilides with moderate to good yields. Inexpensive, safe, and environmentally benign TBHP was proved to be an effective oxidant for these transformations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetanilides / chemistry*
  • Acylation
  • Catalysis
  • Oxidation-Reduction
  • Palladium / chemistry*
  • Stereoisomerism
  • Substrate Specificity
  • Toluene / analogs & derivatives*
  • Toluene / chemistry*

Substances

  • Acetanilides
  • Toluene
  • Palladium