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Reaction of -acetylbenzamides with hydroxylamine hydrochloride: Synthesis of 3-methyl-5-aryl-1,2,4-oxadiazoles

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Arıkan Ölmez, Nevin

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Springer

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A convenient reaction between N-acetylbenzamides and hydroxylamine hydrochloride at 80 degrees C in the presence of pyridine under microwave irradiation was described. This method leads to the formation of 3-methyl-5-aryl-1,2,4-oxadiazole compounds as regioselective in moderate to good yields and also employs simple synthetic protocols devoid of lengthy purification procedures. The reaction was also carried out by both conventional heating and one-pot sequential under microwave irradiation. The structures of synthesized compounds were confirmed by spectroscopic methods.[GRAPHICS].

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One-pot synthesis, Microwave irradiation, 1,2,4-oxadiazoles, Derivatives, Amidoximes, Aldehydes, Nitriles, Imides, Ring, Blue, N-acylbenzamides, Hydroxylamine hydrochloride, 1,2,4-oxadiazole, Microwave-assisted synthesis, Science & technology, Physical sciences, Chemistry, multidisciplinary, Chemistry

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