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Synthesis of Allyl 2-Dialkylamino-4-pentenoates and Their Analogs via Stevens Rearrangement
Authors:Babakhanyan  A V  Shakhbazyan  L G  Grigoryan  Dzh V  Kocharyan  S T
Institution:(1) Abovyan Armenian State Pedagogical University, Zakaria Kanakertsi 167-A, Erevan, 375091, Armenia;(2) Institute of Organic Chemistry, National Academy of Sciences of Armenia, Erevan, Armenia
Abstract:Stevens rearrangement of ammonium salts containing an allyloxycarbonylmethyl group in benzene in the presence of sodium phenoxide yields allyl 2-dialkylamino-4-pentenoates. The rearrangement in the presence of sodium methoxide is accompanied by transesterification to afford methyl 2-dialkylamino-4-pentenoates.
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