Volume 25, Issue 7 pp. 913-916
Full Paper

Electrochemical Dicarboxylation of Styrene: Synthesis of 2-Phenylsuccinic Acid

Huan Wang

Huan Wang

Shanghai Key Laboratory of Green Chemistry and Chemical Process, Department of Chemistry, East China Normal University, Shanghai 200062, China

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Mei-Yu Lin

Mei-Yu Lin

Shanghai Key Laboratory of Green Chemistry and Chemical Process, Department of Chemistry, East China Normal University, Shanghai 200062, China

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Hui-Jue Fang

Hui-Jue Fang

Shanghai Key Laboratory of Green Chemistry and Chemical Process, Department of Chemistry, East China Normal University, Shanghai 200062, China

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Ting-Ting Chen

Ting-Ting Chen

Shanghai Key Laboratory of Green Chemistry and Chemical Process, Department of Chemistry, East China Normal University, Shanghai 200062, China

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Jia-Xing Lu

Jia-Xing Lu

Tel.: 0086-021-62233491; Fax: 0086-021-62232414

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First published: 16 July 2007
Citations: 38

Abstract

Electrochemical dicarboxylation of styrene in the presence of atmospheric pressure of CO2 with a Ti cathode and a Mg rod anode readily took place efficiently in an acetonitrile solution containing 0.1 mol·L−1 tetraethylammonium bromide to give 2-phenylsuccinic acid. Influences of the nature of the electrodes, the current density, the passed charge and the temperature on electrolysis were studied to optimize the electrolytic conditions, with the maximal isolated yield to be 86.07%. The mechanism of the elelctrocarboxylation process has been studied by cyclic voltammetry.

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