Issue 33, 2021

Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution

Abstract

An iron porphyrin-catalyzed N-trifluoroethylation of anilines has been developed with 2,2,2-trifluoroethylamine hydrochloride as the fluorine source. This one-pot N–H insertion reaction is conducted via cascade diazotization/N-trifluoroethylation reactions. The developed transformation can afford a wide range of N-trifluoroethylated anilines in good yields using readily available primary amines and secondary anilines as starting materials.

Graphical abstract: Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution

Supplementary files

Article information

Article type
Paper
Submitted
04 May 2021
Accepted
27 May 2021
First published
07 Jun 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 20322-20325

Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution

S. Ren, G. Xu, Y. Guo, Q. Liu and C. Guo, RSC Adv., 2021, 11, 20322 DOI: 10.1039/D1RA03379D

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