Facile Access to Biaryls and
2-Acetyl-5-arylbenzofurans via Suzuki Coupling in Water under Thermal
and Microwave Conditions

Ahmed F. Darweesh; Mohamed R. Shaaban; Ahmad M. Farag; Peter Metz; Kamal M. Dawood

doi:10.1055/s-0030-1258181

PAPER

Facile Access to Biaryls and 2-Acetyl-5-arylbenzofurans via Suzuki Coupling in Water under Thermal and Microwave Conditions

Ahmed F. Darweesh^a, Mohamed R. Shaaban^a,b, Ahmad M. Farag^a, Peter Metz^c, Kamal M. Dawood*^a
^a Department of Chemistry, Faculty of Science, Cairo University, Giza 12613, Egypt
Fax: +20(2)35727556; e-Mail: dr_dawood@hotmail.com;
^b Department of Chemistry, Faculty of Applied Science, Umm Al-Qura University, Makkah Almukarramah, Saudi Arabia
^c Fachrichtung Chemie und Lebensmittelchemie, Organische Chemie I, Technische Universität Dresden, Bergstraße 66, 01069 Dresden, Germany

Abstract

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Abstract

The phosphine-free Suzuki-Miyaura carbon-carbon cross-coupling reactions of activated and deactivated aryl halides and 2-acetyl-5-bromobenzofuran with various aryl- or heteroarylboronic acids were investigated. A benzothiazole-based palladium(II) complex was used as a precatalyst for the reactions under both thermal and microwave conditions in air using water as a solvent.

Key words

palladium - catalysis - microwave irradiation - Suzuki reactions - benzofuran

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