Issue 21, 2014

Synthesis of N-alkyl isatins via oxidative cyclization of N-alkyl 2-bromo(chloro)acetanilides

Abstract

A highly efficient method for the synthesis of N-alkyl isatins starting from N-alkyl 2-bromo or 2-chloro acetanilides is described. The starting materials are easy to prepare and the yields of isatins are generally high. Operationally the reaction is very simple to run. Even though best results were obtained with a catalytic amount of CuI, the reactions of N-alkyl 2-bromo acetanilides actually performed well even in the absence of any metal catalyst.

Graphical abstract: Synthesis of N-alkyl isatins via oxidative cyclization of N-alkyl 2-bromo(chloro)acetanilides

Supplementary files

Article information

Article type
Communication
Submitted
16 Jan 2014
Accepted
20 Mar 2014
First published
25 Mar 2014

Org. Biomol. Chem., 2014,12, 3349-3353

Synthesis of N-alkyl isatins via oxidative cyclization of N-alkyl 2-bromo(chloro)acetanilides

Q. Gui, F. Dai, J. Liu, P. Chen, Z. Yang, X. Chen and Z. Tan, Org. Biomol. Chem., 2014, 12, 3349 DOI: 10.1039/C4OB00118D

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