Oxidative Esterification of Homologous 1,3-Propanediols

Kotionova, Tatyana, Lee, Christopher, Miedziak, Peter John, Dummer, Nicholas ORCID: https://orcid.org/0000-0002-0946-6304, Willock, David James ORCID: https://orcid.org/0000-0002-8893-1090, Carley, Albert Frederick, Morgan, David John ORCID: https://orcid.org/0000-0002-6571-5731, Knight, David William, Taylor, Stuart H. ORCID: https://orcid.org/0000-0002-1933-4874 and Hutchings, Graham John ORCID: https://orcid.org/0000-0001-8885-1560 2012. Oxidative Esterification of Homologous 1,3-Propanediols. Catalysis Letters 142 (9) , pp. 1114-1120. 10.1007/s10562-012-0872-7

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Abstract

The oxidative esterification of a homologous series of diols (1,3-propanediol,2-methyl-propanediol and 2,2-dimethyl-1,3-propanediol) with methanol has been investigated using titania-supported gold, palladium and gold–palladium catalysts using molecular oxygen. The gold– palladium catalysts showed the highest activity and 1,3-propanediol was the most reactive while the additional methyl groups decreased the reactivity. However, it is possible to achieve high selectivity to methyl 3-hydroxypropionate and 2-methyl-3-hydroxyisobutyrate by mono-oxidations.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Schools > Chemistry Research Institutes & Centres > Cardiff Catalysis Institute (CCI)
Subjects:	Q Science > QD Chemistry
Uncontrolled Keywords:	Gold catalysis;� Gold palladium alloy; nanoparticles; Oxidative esterification; Diol oxidation
Publisher:	Springer
ISSN:	1011-372X
Last Modified:	06 May 2023 01:28
URI:	https://orca.cardiff.ac.uk/id/eprint/38890

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