The Catalytic Reduction of Aldehydes and Ketones with 2-Propanol over Hydrous Zirconium Oxide

Abstract

Reduction of aldehydes with 2-propanol proceeded efficiently by catalysis with hydrous zirconium oxide to give the corresponding alcohols. Most ketones also were reduced efficiently, but conjugated or sterically hindered ketones resisted the reduction. The reduction was carried out with primary, secondary, or tertiary alcohols, and only secondary alcohols served as hydrogen donors. Kinetic experiments have indicated that the reaction rate is of first-order dependence on each of the concentrations of the carbonyl compound, 2-propanol, and the catalyst. An observation of the primary isotope effect has suggested that a step of hydride transfer from absorbed 2-propanol to absorbed carbonyl compound constitutes the rate-determining step for the reduction.