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SYNTHESIS OF 2-AMINOTHIAZOLIDIN-4-ONES FROM (HEPTA-O-ACETYL-b-MALTOSYL)THIOSEMICARBAZONES OF SUBSTITUTED ACETOPHENONES
Published:
30 October 2015
by MDPI
in The 19th International Electronic Conference on Synthetic Organic Chemistry
session Ionic Liquids
Abstract:
Reaction of substituted acetophenone (hepta-O-acetyl-b-maltosyl)thiosemicarbazones with ethyl bromoacetate was investigated. It’s indicated that the nature of solvents and the catalysts affected the reaction yields, and that the microwave-assisted heating method gave higher yields of products than the conventional heating one. Based on the optimum conditions, ionic liquid [HOCH2CH2NH3+]‒OAc, dried chloroform and microwave-assisted heating, the synthesis of some 2-iminothiazolidin-4-ones containg maltose moiety were synthesized. Their structure have been confirmed by spectral data (FTIR, 1H NMR, 13C NMR and MS).
Keywords: Ionic liquid, 2-Iminothiazolidin-4-one, β-Maltose, Microwave-assisted, Thiosemicarbazones
Comments on this paper
Julio A. Seijas
2 November 2015
MW conditions
Dear Dr. Thanh,
which are the microwave irradiation conditions (power, temperature) and the type of microwave oven used?
thanks
jasv
which are the microwave irradiation conditions (power, temperature) and the type of microwave oven used?
thanks
jasv