Synlett 2014; 25(20): 2903-2907
DOI: 10.1055/s-0034-1378903
letter
© Georg Thieme Verlag Stuttgart · New York

Selective Azidation of Aryl Halides to Aryl Azides Promoted by Proline and CuFeO2

Abdol Reza Hajipour*
a  Pharmaceutical Research Laboratory, Department of Chemistry, Isfahan University of Technology, Isfahan 84156, Iran   Fax: +98(311)3912350   Email: haji@cc.iut.ac.ir
b  Department of Neuroscience, University of Wisconsin, Medical School, 1300 University Avenue, Madison, WI 53706-1532, USA
,
Morteza Karimzadeh
a  Pharmaceutical Research Laboratory, Department of Chemistry, Isfahan University of Technology, Isfahan 84156, Iran   Fax: +98(311)3912350   Email: haji@cc.iut.ac.ir
,
Sirous Ghorbani
› Author Affiliations
Further Information

Publication History

Received: 16 July 2014

Accepted after Revision: 30 September 2014

Publication Date:
29 October 2014 (online)


Abstract

An efficient and selective azidation of aryl halides by reacting sodium azide with aryl halides is described. The heterogeneous nature of the copper(Ι) catalyst, which catalyzes the cross-coupling reactions, and the antiviral and antibacterial properties of the products are features of this methodology. It is also worth noting that no aryl amines are produced as byproducts under these conditions.

Supporting Information

 
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