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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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 |
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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 |
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