Issue 7, 2012

Metal triflate catalysed acetal exchange reactions of glycerol under solvent-free conditions

Abstract

Catalytic quantities of indium(III) triflate (In(OTf)3) efficiently promote transacetalisation reactions of glycerol with acyclic acetals to generate the corresponding cyclic acetals under solvent-free reaction conditions. The protocol is rapid and employs very mild reaction conditions. Unreactive ketones, such as acetophenone or benzophenone, undergo efficient acetalisation in the presence of In(OTf)3 and trimethyl orthoformate (TMOF) to give high conversions of the corresponding glycerol acetals.

Graphical abstract: Metal triflate catalysed acetal exchange reactions of glycerol under solvent-free conditions

Article information

Article type
Communication
Submitted
17 Jan 2012
Accepted
17 Jan 2012
First published
21 Feb 2012

RSC Adv., 2012,2, 2702-2706

Metal triflate catalysed acetal exchange reactions of glycerol under solvent-free conditions

B. M. Smith, T. M. Kubczyk and A. E. Graham, RSC Adv., 2012, 2, 2702 DOI: 10.1039/C2RA20100C

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