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Baeyer-Viiliger Oxidation of Cyclic Ketones Using Aqueous Hydrogen Peroxide Catalyzed by Heteropolyacids in Solvent-free System

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Published/Copyright: November 30, 2016
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Abstract

The conversion of cyclic ketones to lactones was catalyzed by different acid catalysts using aqueous hydrogen peroxide (30 wt%) as a clean oxidant. H3PW12O40 seems to be a rather efficient and highly selective catalyst for the Baeyer-Villiger reaction of 2-heptylcyclopentanone and 2-adamantanone to lactones. For cyclopentanone, cyclohexanone, cycloheptanone and cyclododecanone, the selectivity for lactones was very poor, but selectivity for acids was high.

Received: 2013-11-5
Revised: 2014-1-17
Accepted: 2014-1-20
Published Online: 2016-11-30
Published in Print: 2014-7-1

© 2016 by Walter de Gruyter Berlin/Boston

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