Issue 4, 2020

Transition metal- and solvent-free double hydroboration of nitriles

Abstract

A highly efficient, room temperature double hydroboration of nitriles under transition metal-free and solvent-free conditions is reported. Sodium triethylborohydride is used as a catalyst and yields up to 99% are disclosed. Mechanistic studies reveal the reaction proceeds in a stepwise manner with initial formation of a boryl-imine which undergoes a second hydroboration to afford a diborylated amine product.

Graphical abstract: Transition metal- and solvent-free double hydroboration of nitriles

Supplementary files

Article information

Article type
Communication
Submitted
13 Dec 2019
Accepted
29 Jan 2020
First published
29 Jan 2020

Green Chem., 2020,22, 1125-1128

Author version available

Transition metal- and solvent-free double hydroboration of nitriles

D. Bedi, A. Brar and M. Findlater, Green Chem., 2020, 22, 1125 DOI: 10.1039/C9GC04260A

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