Copper(II) Acetate/1,4-Diphenyl-1,4-diazabuta-1,3-diene Catalyzed Sonogashira Cross-Coupling of Aryl Halides with Terminal Alkynes under Aerobic and Solvent-Free Conditions

Chen-Liang Deng; Ye-Xiang Xie; Du-Lin Yin; Jin-Heng Li

doi:10.1055/s-2006-950207

PAPER

Copper(II) Acetate/1,4-Diphenyl-1,4-diazabuta-1,3-diene Catalyzed Sonogashira Cross-Coupling of Aryl Halides with Terminal Alkynes under Aerobic and Solvent-Free Conditions

Chen-Liang Deng, Ye-Xiang Xie, Du-Lin Yin, Jin-Heng Li*
Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research (Ministry of Education), College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, P. R. of China
Fax: +86(731)8872531; e-Mail: jhli@hunnu.edu.cn;

Abstract

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Abstract

The Sonogashira cross-coupling of aryl halides with terminal alkynes catalyzed by an inexpensive copper(II) acetate/1,4-diphenyl-1,4-diazabuta-1,3-diene [Cu(OAc)₂/DAB-Ph] catalytic system is reported. A series of ligands, including diazabutadiene systems, N,N-dimethylglycine, l-proline, ethylenediamine, and phosphines, were evaluated, and 1,4-diphenyl-1,4-diazabuta-1,3-diene provided the best results. In the presence of copper(II) acetate (10 mol%), 1,4-diphenyl-1,4-diazabuta-1,3-diene (20 mol%), and tetrabutylammonium fluoride (3 equiv), a number of aryl iodides or bromides were treated smoothly with alkynes to afford the corresponding products in moderate to excellent yields. It is noteworthy that the reaction is conducted under aerobic and solvent-free conditions.

Key words

copper(II) acetate - diazabutadiene - Sonogashira cross-coupling reaction - aryl halide - terminal alkyne

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Referenzen

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