Highly efficient selective oxidation of alcohols to carbonyl compounds catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen

Bioorg Med Chem Lett. 2007 Nov 15;17(22):6364-8. doi: 10.1016/j.bmcl.2007.08.063. Epub 2007 Aug 28.

Abstract

Efficient selective oxidation of alcohols to carbonyl compounds by molecular oxygen with isobutyraldehyde as oxygen acceptor in the presence of metalloporphyrins has been reported. Ruthenium (III) meso-tetraphenylporphyrin chloride (Ru(TPP)Cl) showed excellent activity and selectivity for oxidation of various alcohols under mild conditions. Moreover, different factors influencing alcohols oxidation, for example, catalyst, solvent, temperature, and oxidant, have been investigated. In large-scale oxidation of benzyl alcohol, the isolated yield of benzaldehyde of 89% was observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemistry*
  • Catalysis
  • Metalloporphyrins / chemistry*
  • Molecular Structure
  • Oxidation-Reduction
  • Oxygen / chemistry*
  • Oxygen / metabolism
  • Ruthenium / chemistry*

Substances

  • Alcohols
  • Metalloporphyrins
  • ruthenium (III) meso-tetraphenylporphyrin chloride
  • Ruthenium
  • Oxygen