4.7 Article

Electrochemical oxidation of some dihydroxybenzene derivatives in the presence of indole

Journal

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
Volume 616, Issue 1-2, Pages 79-86

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2008.01.012

Keywords

Michael reaction; cyclic voltammetry; indole; benzoquinone; 2,5-dihydroxybenzoic acid

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The present work explains electrochemical behavior of some dihydroxybenzoic acid and catechol derivatives (1a-d) in the presence of indole (3) as a nucleophile using cyclic voltammetry and controlled-potential coulometry methods and describes a new electrochemical strategy for the synthesis of some new indolyl derivatives of quinones and catechols. In this work, we derive these products with good yields based on electrochemical oxidation under controlled potential conditions in aqueous solutions, without toxic reagents and solvents at a carbon electrode, using an environmentally friendly method. (c) 2008 Elsevier B.V. All rights reserved.

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