Manganese-catalyzed selective oxidation of aliphatic C-H groups and secondary alcohols to ketones with hydrogen peroxide

ChemSusChem. 2013 Sep;6(9):1774-8. doi: 10.1002/cssc.201300378. Epub 2013 Sep 5.

Abstract

An efficient and simple method for selective oxidation of secondary alcohols and oxidation of alkanes to ketones is reported. An in situ prepared catalyst is employed based on manganese(II) salts, pyridine-2-carboxylic acid, and butanedione, which provides good-to-excellent conversions and yields with high turnover numbers (up to 10 000) with H2 O2 as oxidant at ambient temperatures. In substrates bearing multiple alcohol groups, secondary alcohols are converted to ketones selectively and, in general, benzyl C-H oxidation proceeds in preference to aliphatic C-H oxidation.

Keywords: alcohol oxidation; alkane oxidation; catalysis; manganese.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemistry*
  • Carbon / chemistry*
  • Catalysis
  • Hydrogen / chemistry*
  • Hydrogen Peroxide / chemistry*
  • Ketones / chemistry*
  • Manganese / chemistry*
  • Oxidation-Reduction
  • Substrate Specificity

Substances

  • Alcohols
  • Ketones
  • Manganese
  • Carbon
  • Hydrogen
  • Hydrogen Peroxide