4.2 Article

Iodine (III)-mediated one-pot synthesis of quinoxaline by tandem nucleophilic substitution and cyclisation

Journal

JOURNAL OF CHEMICAL RESEARCH
Volume -, Issue 10, Pages 605-607

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.3184/174751911X13181827496987

Keywords

quinoxaline; acetophenones; o-phenylenediamines; [hydroxy(tosyloxy)iodo]benzene; nitrogen-containing heterocycles

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Quinoxaline derivatives are widely used in dyes, electroluminescent materials and organic semiconductors. An economic and convenient strategy for the synthesis of 2-phenyl-quinoxaline is described. The approach relies on the oxidation of acetophenones by [hydroxy(tosyloxy)iodo] benzene, followed by tandem nucleophilic substitution with o-phenylenediamines, dehydration cyclisation and dehydrogenation. The method was performed in two stages as a one-pot reaction.

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