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A GREEN METHOD FOR THE SYNTHESIS OF -ARYLBENZOTHIAZOLES

机译:合成芳基噻唑的绿色方法

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摘要

Aromatic aldehydes with both electron withdrawing and electron donating substituents were smoothly converted to the corresponding 2-arylbenzothiazoles by direct condensation of aromatic aldehydes with 2-aminothiophenol in one pot in a microoven under solvent-free conditions without any catalyst.The study revealed that the synthesis proceeded in three stages;first the formation of the aryl imine followed by its cyclisation to the benzothiazoline which in turn underwent oxidation and dehydration to the final product benzothiazole.Isolation of intermediates in all the stages confirmed the mechanism.This is therefore the first report of a "green" synthesis of the 2-arylbenzothiazoles under solvent-free conditions in the absence of any catalyst.
机译:在无溶剂条件下,在无溶剂的条件下,在一个锅中于无溶剂的条件下,将芳香醛与2-氨基苯硫酚直接缩合,将具有吸电子和供电子取代基的芳香醛平稳地转化为相应的2-芳基苯并噻唑。整个过程分为三个阶段:首先形成芳基亚胺,然后环化成苯并噻唑啉,然后再进行氧化和脱水生成最终产物苯并噻唑,所有阶段的中间体分离均证实了这一机理,因此这是第一个报道在没有任何催化剂的情况下,在无溶剂条件下2-芳基苯并噻唑的“绿色”合成。

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