Issue 10, 2021, Issue in Progress

Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives

Abstract

We describe copper-catalyzed cyanomethylation of imines and α,β-alkenes with a methylnitrile source and provide an efficient route to synthesize arylacrylonitriles and β,γ-unsaturated nitriles. This method tolerates aliphatic and aromatic alkenes substituted with a variety of functional groups such as F, Cl, Br, Me, OMe, tert-Bu, NO2, NH2 and CO2H with good to excellent yields (69–98%). These systems consist of inexpensive, simple copper catalyst and acetonitrile with its derivatives (α-bromo/α-iodo-acetonitrile) and are highly applicable in the industrial production of acrylonitriles.

Graphical abstract: Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives

Supplementary files

Article information

Article type
Paper
Submitted
21 Dec 2020
Accepted
19 Jan 2021
First published
28 Jan 2021
This article is Open Access
Creative Commons BY license

RSC Adv., 2021,11, 5427-5431

Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives

M. S. Ahmad and A. Ahmad, RSC Adv., 2021, 11, 5427 DOI: 10.1039/D0RA10693C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements