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Home / Phosphorus, Sulfur, and Silicon and the Related Elements, Volume 181, Number 6

Diaryl Sulfones Through Oxidative Coupling of Catechols and Arylsulfinic Acids

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A simple and efficient method for the synthesis of diaryl sulfones using the coupling reaction of in-situ generated o -benzoquinones, promoted by potassium ferricyanide, and arylsulfinic acids has been developed. High product yields, a short reaction time, and mild reaction conditions are important features of this method.

Keywords: Catechols; diaryl sulfones; o-benzoquinones; oxidative coupling; potassium ferricyanide

Document Type: Research Article

Affiliations: 1: Department of Chemistry, Bu-Ali Sina University, Hamadan, Iran 2: Department of Chemistry, Razi University, Kermanshah, Iran

Publication date: 01 June 2006

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