Issue 49, 2021

Metal-free site-selective C–H cyanoalkylation of 8-aminoquinoline and aniline-derived amides with azobisisobutyronitrile

Abstract

Using K2S2O8, an efficient and metal-free site-selective C–H cyanoalkylation of 8-aminoquinoline and aniline-derived amides with AIBN (azobisisobutyronitrile) was developed. Without any catalyst, various substrates and functional groups were compatible to afford corresponding products in moderate to high yields. A mechanism study displayed that a radical–radical coupling process was involved via the N-centered radical generation and delocalization of aryl amides.

Graphical abstract: Metal-free site-selective C–H cyanoalkylation of 8-aminoquinoline and aniline-derived amides with azobisisobutyronitrile

Supplementary files

Article information

Article type
Paper
Submitted
09 Aug 2021
Accepted
25 Aug 2021
First published
15 Sep 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 30719-30724

Metal-free site-selective C–H cyanoalkylation of 8-aminoquinoline and aniline-derived amides with azobisisobutyronitrile

M. Zhao, Z. Qin, K. Zhang and J. Li, RSC Adv., 2021, 11, 30719 DOI: 10.1039/D1RA06013A

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