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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 |
Sumario: | 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. |
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