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Water-Promoted Mild and General Michaelis–Arbuzov Reaction of Triaryl Phosphites and Aryl Iodides by Palladium Catalysis

Jin Zhang, Wei Hu, Zihan Chen, Nuo Wu, Chunya Li, Tieqiao Chen, Li‐Biao Han

2024Organic Letters10 citationsDOI

Abstract

A Pd-catalyzed relatively general Michaelis-Arbuzov reaction of triaryl phosphites and aryl iodides for preparing useful aryl phosphonates was developed. Interestingly, water can greatly facilitate the reaction through a water-participating phosphonium intermediate rearrangement process, which also makes the reaction conditions rather mild. In comparison with the known methods, this reaction is milder and more general, as it exhibits excellent functional group tolerance, can be applied to various triaryl phosphites and aryl iodides, and can be extended to aryl phosphonites and phosphinites. A gram-scale reaction with a low catalyst loading also revealed its practicality and potential in large-scale preparation.

Topics & Concepts

ChemistryArylCatalysisPalladiumPhosphoniumReaction conditionsPalladium catalystOrganic chemistryCombinatorial chemistryAlkylCatalytic Cross-Coupling ReactionsOrganophosphorus compounds synthesisSulfur-Based Synthesis Techniques
Water-Promoted Mild and General Michaelis–Arbuzov Reaction of Triaryl Phosphites and Aryl Iodides by Palladium Catalysis | Litcius