Issue 24, 2014

Palladium-catalyzed tandem reaction of 2-hydroxyarylacetonitriles with sodium sulfinates: one-pot synthesis of 2-arylbenzofurans

Abstract

The first example of the palladium-catalyzed one-pot synthesis of 2-arylbenzofurans in moderate to excellent yields via a tandem reaction of 2-hydroxyarylacetonitriles with sodium sulfinates is reported. A plausible mechanism for the formation of 2-arylbenzofurans involving desulfinative addition and intramolecular annulation reactions is proposed. Moreover, the present synthetic route to benzofurans could be readily scaled up to the gram quantity without any difficulty. Thus, the method represents a convenient and practical strategy for synthesis of benzofuran derivatives.

Graphical abstract: Palladium-catalyzed tandem reaction of 2-hydroxyarylacetonitriles with sodium sulfinates: one-pot synthesis of 2-arylbenzofurans

Supplementary files

Article information

Article type
Communication
Submitted
17 Mar 2014
Accepted
23 Apr 2014
First published
24 Apr 2014

Org. Biomol. Chem., 2014,12, 4078-4083

Author version available

Palladium-catalyzed tandem reaction of 2-hydroxyarylacetonitriles with sodium sulfinates: one-pot synthesis of 2-arylbenzofurans

J. Chen, J. Li and W. Su, Org. Biomol. Chem., 2014, 12, 4078 DOI: 10.1039/C4OB00575A

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