Issue 19, 2021

CO2-tuned highly selective reduction of formamides to the corresponding methylamines

Abstract

We herein describe an efficient, CO2-tuned and highly selective C–O bond cleavage of N-methylated formanilides. With easy-to-handle and commercially available NaBH4 as the reductant, a variety of formanilides could be turned into the desired tertiary amines in moderate to excellent yields. The role of CO2 has been investigated in detail, and the mechanism is proposed on the basis of experiments.

Graphical abstract: CO2-tuned highly selective reduction of formamides to the corresponding methylamines

Supplementary files

Article information

Article type
Communication
Submitted
06 Aug 2021
Accepted
03 Sep 2021
First published
03 Sep 2021

Green Chem., 2021,23, 7534-7538

CO2-tuned highly selective reduction of formamides to the corresponding methylamines

Z. Guo, T. Pang, L. Yan, X. Wei, J. Chao and C. Xi, Green Chem., 2021, 23, 7534 DOI: 10.1039/D1GC02815D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements