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Electrochemical Dicarboxylation of Styrene: Synthesis of 2-Phenylsuccinic Acid

✍ Scribed by Huan Wang; Mei-Yu Lin; Hui-Jue Fang; Ting-Ting Chen; Jia-Xing Lu


Book ID
102101957
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
51 KB
Volume
25
Category
Article
ISSN
0256-7660

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✦ Synopsis


Abstract

Electrochemical dicarboxylation of styrene in the presence of atmospheric pressure of CO~2~ with a Ti cathode and a Mg rod anode readily took place efficiently in an acetonitrile solution containing 0.1 molΒ·L^βˆ’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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A 2-propanol solvate of (RS)-phenylΒ­succ
✍ Fischer, Andreas ;Profir, Veronica M. πŸ“‚ Article πŸ“… 2004 πŸ› International Union of Crystallography 🌐 English βš– 210 KB

A solvate of (RS)-phenylsuccinic acid (RS-PSA) has been obtained from 2-propanol (IPA). The compound, C 10 H 10 O 4 ÁC 3 H 8 O, crystallizes in the monoclinic crystal system (space group C2/c). It features molecules of the S form of the acid, one of whose carboxy groups is connected to one carboxy g