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Electrochemically initiated oxidative cyclization: a versatile route for the synthesis of 5-substituted 2-amino-1,3,4-oxadiazoles

机译:电化学引发的氧化环化:合成5-取代的2-氨基-1,3,4-恶二唑的通用途径

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摘要

A rapid, improved, and environmentally benign synthesis of 5-substituted 2-amino-1,3,4-oxadiazoles by one-pot electrocyclization of acylthiosemicarbazones is reported. Controlled potential electrolysis was performed at room temperature in acetonitrile as non-aqueous solvent and LiClO4 as supporting electrolyte. The reaction products were characterized by spectroscopic methods and a mechanism was deduced from voltammetric data. Better yields at room temperature, shortest reaction time, and easy work-up are attractive features of this green procedure.
机译:据报道,通过一锅法电化酰基硫代半咪唑酮,可以快速,改进且对环境无害,可以合成5-取代的2-氨基-1,3,4-恶二唑。在室温下在乙腈中作为非水溶剂,在LiClO4中作为辅助电解质,进行受控电势电解。通过光谱法表征反应产物,并从伏安数据推导其机理。室温下的高收率,最短的反应时间和易于后处理是这种绿色工艺的诱人之处。

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