Issue 10, 2013

Merging the ring opening of benzoxazoles with secondary amines and an iron-catalyzed oxidative cyclization towards the environmentally friendly synthesis of 2-aminobenzoxazoles

Abstract

A facile and environmentally friendly method was developed through merging the ring opening of benzoxazoles with secondary amines and an iron-catalyzed oxidative cyclization towards the synthesis of 2-aminobenzoxazoles. In the oxidative cyclization step, with catalytic amounts of FeCl and aqueous H2O2 as a green oxidant, highly desirable 2-aminobenzoxazoles were isolated in excellent yields of up to 97%. A plausible radical process is proposed for the oxidative cyclization on the basis of mechanistic studies.

Graphical abstract: Merging the ring opening of benzoxazoles with secondary amines and an iron-catalyzed oxidative cyclization towards the environmentally friendly synthesis of 2-aminobenzoxazoles

Supplementary files

Article information

Article type
Paper
Submitted
21 Jun 2013
Accepted
02 Aug 2013
First published
06 Aug 2013

Green Chem., 2013,15, 2975-2980

Merging the ring opening of benzoxazoles with secondary amines and an iron-catalyzed oxidative cyclization towards the environmentally friendly synthesis of 2-aminobenzoxazoles

D. Xu, W. Wang, C. Miao, Q. Zhang, C. Xia and W. Sun, Green Chem., 2013, 15, 2975 DOI: 10.1039/C3GC41206G

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