Issue 29, 2016

P4 functionalization by hydrides: direct synthesis of P–H bonds

Abstract

A direct method for white phosphorus functionalization by hydride sources is presented. Excess BH4 in n-butylamine produces HP4 as the major P-containing species. Reaction with LiBEt3H forms the borane-stabilized phosphanide Li(PH2)(BEt3)2, which may be used to synthesize various phosphines. Triethylborane may be replaced by BH3, resulting in the formation of LiPH2(BH3)2.

Graphical abstract: P4 functionalization by hydrides: direct synthesis of P–H bonds

Supplementary files

Article information

Article type
Communication
Submitted
24 Feb 2016
Accepted
15 Mar 2016
First published
16 Mar 2016

Chem. Commun., 2016,52, 5179-5182

P4 functionalization by hydrides: direct synthesis of P–H bonds

K. X. Bhattacharyya, S. Dreyfuss, N. Saffon-Merceron and N. Mézailles, Chem. Commun., 2016, 52, 5179 DOI: 10.1039/C6CC01683A

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