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

Abstract

Abstract 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.