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First reusable ligand-free palladium catalyzed C–P bond formation of aryl halides with trialkylphosphites in neat water†
Nasser Iranpoor,Habib Firouzabadi,Khashayar Rajabi Moghadam,Somayeh Motavalli
RSC Advances Pub Date : 10/07/2014 00:00:00 , DOI:10.1039/C4RA07680J
Abstract

A reusable ligand-free palladium catalyzed phosphonation of aryl iodides, bromides and chlorides with trialkylphosphites is described for the first time in neat water. The aryl phosphonates are obtained in good to excellent yields. The reaction can be also performed with Ni(II) with longer reaction time. The role of tetrabutylammonium bromide in this reaction as reducing agent for generation of Pd(0) at room temperature is also demonstrated. Pd(0)/TBAB was easily reused for three runs without decreasing the efficiency.

Graphical abstract: First reusable ligand-free palladium catalyzed C–P bond formation of aryl halides with trialkylphosphites in neat water
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