Base-free direct oxidation of 1-octanol to octanoic acid and its octyl ester over supported gold catalysts

ChemSusChem. 2012 Nov;5(11):2243-8. doi: 10.1002/cssc.201200324. Epub 2012 Oct 12.

Abstract

The choice of a suitable support for gold nanoparticles (Au NPs) enabled the direct oxidation of unreactive aliphatic alcohol, 1-octanol, to octanoic acid and octyl octanoate in the absence of a base. Under optimized conditions, Au NPs supported on NiO (Au/NiO) exhibited remarkably high catalytic activities and excellent selectivities to octanoic acid (e.g., 97 %) at full conversion. In contrast to Au/NiO, Au/CeO₂ selectively produced octyl octanoate as a major product in a base-free aqueous solution with a maximum selectivity of 82 % under optimized conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Octanol / chemistry*
  • Caprylates / chemistry*
  • Catalysis
  • Cerium / chemistry
  • Esters
  • Gold / chemistry*
  • Nickel / chemistry
  • Oxidation-Reduction

Substances

  • Caprylates
  • Esters
  • Cerium
  • ceric oxide
  • Gold
  • Nickel
  • nickel monoxide
  • 1-Octanol
  • octanoic acid