48 / 2023-08-14 10:20:58
Photochemical Benzylation of White Phosphorus
White Phosphorus,Benzylation,Wittig reagent
Abstract Accepted
Xinlei Huangfu / Peking University;College of Chemistry
Wei Liu / Peking University;College of Chemistry
Hanhua Xu / Peking University;College of Chemistry
Zhongzhen Wang / Peking University;College of Chemistry
Junnian Wei / Peking University;College of Chemistry
Wen-Xiong Zhang / Peking University;College of Chemistry
White phosphorus (P4) acts as a starting industrial material for the large-scale preparation of organophosphorus compounds (OPCs) via a classical P4→PCl3→OPCs route. From the economic and waste-disposal viewpoints, the direct functionalization of P4 without chlorination to construct P−C bonds is of great significance.[1] The traditional synthesis for benzyltriphenylphosphonium salts involves the chlorination of P4, substitution by metal reagents and nucleophilic substitution of halogenated hydrocarbons.[2] Herein, we report photochemical benzylation of P4 to construct tetrabenzylphosphonium bromide directly. The tetrabenzylphosphonium salts can be used instead of the benzyltriphenylphosphonium salts in Wittig reaction, which was a commonly Wittig reagent for converting benzaldehyde to styrene derivatives.[3]

 
Important Date
  • Conference Date

    Nov 12

    2023

    to

    Nov 16

    2023

  • Oct 24 2023

    Draft paper submission deadline

  • Nov 16 2023

    Registration deadline

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Ningbo University
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