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Updated: Jun 9, 2025

Preparation and Use of Carbonyl-decorated Carbenes in the Activation of White Phosphorus
Published on: October 3, 2014
Selective Functionalization of White Phosphorus with Alkyl Bromides under Photocatalytic Conditions: A Chlorine-Free
Jialiang Peng1, An Wang1, Yan Liu1
1Department of Chemistry, College of Chemistry and Chemical Engineering, and the Key Laboratory for Chemical Biology of Fujian Province, Xiamen University, Xiamen, Fujian 361005, China.
Abstract:
A novel and efficient method for the direct selective alkylation of white phosphorus (P4) with alkyl bromides has been developed, utilizing 4DPAIPN as the photocatalyst and Hantzsch ester as the reductant. This method facilitates the synthesis of structurally diverse dialkyl phosphine oxides in good yields, offering a streamlined alternative to the traditional stepwise approach of chlorinating P4 with Cl2 and subsequently displacing the chlorine atom. Noteworthy features of this reaction include excellent product selectivity, remarkable functional group tolerance, and a broad substrate scope. Additionally, this method is effective for the synthesis of trialkyl phosphine oxides.
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