Cargando…

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

For over half a century, thousands of tons of triphenylphosphine oxide Ph(3)P(O) have been produced every year from the chemical industries as a useless chemical waste. Here we disclose efficient transformations of Ph(3)P(O) with cheap resource-abundant metallic sodium finely dispersed in paraffin o...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Jian-Qiu, Ye, Jingjing, Huang, Tianzeng, Shinohara, Hiroyuki, Fujino, Hiroyoshi, Han, Li-Biao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812262/
https://www.ncbi.nlm.nih.gov/pubmed/36703346
http://dx.doi.org/10.1038/s42004-019-0249-6
_version_ 1784863690974035968
author Zhang, Jian-Qiu
Ye, Jingjing
Huang, Tianzeng
Shinohara, Hiroyuki
Fujino, Hiroyoshi
Han, Li-Biao
author_facet Zhang, Jian-Qiu
Ye, Jingjing
Huang, Tianzeng
Shinohara, Hiroyuki
Fujino, Hiroyoshi
Han, Li-Biao
author_sort Zhang, Jian-Qiu
collection PubMed
description For over half a century, thousands of tons of triphenylphosphine oxide Ph(3)P(O) have been produced every year from the chemical industries as a useless chemical waste. Here we disclose efficient transformations of Ph(3)P(O) with cheap resource-abundant metallic sodium finely dispersed in paraffin oil. Ph(3)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(3)P(O) to be used as a precious starting material for highly valuable phosphorus compounds.
format Online
Article
Text
id pubmed-9812262
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-98122622023-01-10 Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium Zhang, Jian-Qiu Ye, Jingjing Huang, Tianzeng Shinohara, Hiroyuki Fujino, Hiroyoshi Han, Li-Biao Commun Chem Article For over half a century, thousands of tons of triphenylphosphine oxide Ph(3)P(O) have been produced every year from the chemical industries as a useless chemical waste. Here we disclose efficient transformations of Ph(3)P(O) with cheap resource-abundant metallic sodium finely dispersed in paraffin oil. Ph(3)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(3)P(O) to be used as a precious starting material for highly valuable phosphorus compounds. Nature Publishing Group UK 2020-01-03 /pmc/articles/PMC9812262/ /pubmed/36703346 http://dx.doi.org/10.1038/s42004-019-0249-6 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Jian-Qiu
Ye, Jingjing
Huang, Tianzeng
Shinohara, Hiroyuki
Fujino, Hiroyoshi
Han, Li-Biao
Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium
title Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium
title_full Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium
title_fullStr Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium
title_full_unstemmed Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium
title_short Conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of C-P, O-P, and C-H bonds with sodium
title_sort conversion of triphenylphosphine oxide to organophosphorus via selective cleavage of c-p, o-p, and c-h bonds with sodium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812262/
https://www.ncbi.nlm.nih.gov/pubmed/36703346
http://dx.doi.org/10.1038/s42004-019-0249-6
work_keys_str_mv AT zhangjianqiu conversionoftriphenylphosphineoxidetoorganophosphorusviaselectivecleavageofcpopandchbondswithsodium
AT yejingjing conversionoftriphenylphosphineoxidetoorganophosphorusviaselectivecleavageofcpopandchbondswithsodium
AT huangtianzeng conversionoftriphenylphosphineoxidetoorganophosphorusviaselectivecleavageofcpopandchbondswithsodium
AT shinoharahiroyuki conversionoftriphenylphosphineoxidetoorganophosphorusviaselectivecleavageofcpopandchbondswithsodium
AT fujinohiroyoshi conversionoftriphenylphosphineoxidetoorganophosphorusviaselectivecleavageofcpopandchbondswithsodium
AT hanlibiao conversionoftriphenylphosphineoxidetoorganophosphorusviaselectivecleavageofcpopandchbondswithsodium