Issue 11, 2022

9-BBN and chloride catalyzed reduction of chlorophosphines to phosphines and diphosphines

Abstract

The commercially available Lewis acid, 9-BBN and Lewis basic [Et4N]Cl are used as catalysts for the reduction of chlorophosphines R2PCl in the presence of phenylsilane. Aryl-chlorophosphines afford primarily diphosphines (P2R4) while secondary phosphines predominate for alkyl-substituted precursors. Use of the combined catalysts leads to reduced reaction time and temperature, providing a rapid, scalable, and facile protocol for the preparation of diphosphines or secondary phosphines.

Graphical abstract: 9-BBN and chloride catalyzed reduction of chlorophosphines to phosphines and diphosphines

Supplementary files

Article information

Article type
Communication
Submitted
15 Nov 2021
Accepted
10 Jan 2022
First published
10 Jan 2022

Chem. Commun., 2022,58, 1740-1743

9-BBN and chloride catalyzed reduction of chlorophosphines to phosphines and diphosphines

I. Elser, R. J. Andrews and D. W. Stephan, Chem. Commun., 2022, 58, 1740 DOI: 10.1039/D1CC06439H

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