Bulletin of the Chemical Society of Japan p. 3283 - 3288 (1988)
Update date:2022-08-17
Topics:
Shibagaki, Makoto
Takahashi, Kyoko
Matasushita, Hajime
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 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.
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