Synthesis of esters from acyl chlorides and halide under solid-liquid phase transfer catalysis

Article abstract of DOI:10.1080/00397919208021541

A new and general method for the synthesis of esters is reported. Acyl chloride reacts with halide in the presence of hydrogen carbonate and under solid-liquid phase transfer condition to afford the esters in good to excellent isolated yields. The effects of catalyst, sodium and solvents to the reactions have been investigated. The reaction mechanism is briefly discussed.

Full text of DOI:10.1080/00397919208021541

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Synthetic Communications: An
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Organic Chemistry
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Synthesis of Esters from Acyl
Chlorides and Halide Under
Solid-Liquid Phase Transfer
Catalysis
Yulai Hu a , Weihua Pa b , Wenfeng Cui a & Jinxian
Wang a
a Institute of Chemistry, Department of Chemistry ,
Northwest Normal University , 95 An Nin Road(E.),
730070, Lanzhou, China
b Lanzhou Railway College , 790070, Lanzhou, China
Published online: 23 Sep 2006.
To cite this article: Yulai Hu , Weihua Pa , Wenfeng Cui & Jinxian Wang (1992)
Synthesis of Esters from Acyl Chlorides and Halide Under Solid-Liquid Phase
Transfer Catalysis, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 22:19, 2763-2767, DOI:
10.1080/00397919208021541
To link to this article: http://dx.doi.org/10.1080/00397919208021541
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