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Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium.

Authors :
Zhang JQ
Ye J
Huang T
Shinohara H
Fujino H
Han LB
Source :
Communications chemistry [Commun Chem] 2020 Jan 03; Vol. 3 (1), pp. 1. Date of Electronic Publication: 2020 Jan 03.
Publication Year :
2020

Abstract

For over half a century, thousands of tons of triphenylphosphine oxide Ph <subscript>3</subscript> P(O) have been produced every year from the chemical industries as a useless chemical waste. Here we disclose efficient transformations of Ph <subscript>3</subscript> P(O) with cheap resource-abundant metallic sodium finely dispersed in paraffin oil. Ph <subscript>3</subscript> P(O) can be easily and selectively transformed to three reactive organophosphorus intermediates-sodium diphenylphosphinite, sodium 5H-benzo[b]phosphindol-5-olate and sodium benzo[b]phosphindol-5-ide-that efficiently give the corresponding functional organophosphorus compounds in good yields. These functional organophosphorus compounds are difficult to prepare but highly industrially useful compounds. This may allow Ph <subscript>3</subscript> P(O) to be used as a precious starting material for highly valuable phosphorus compounds.<br /> (© 2020. The Author(s).)

Details

Language :
English
ISSN :
2399-3669
Volume :
3
Issue :
1
Database :
MEDLINE
Journal :
Communications chemistry
Publication Type :
Academic Journal
Accession number :
36703346
Full Text :
https://doi.org/10.1038/s42004-019-0249-6