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Green Synthesis of Halogenated Thiophenes Selenophenes and Benzobselenophenes Using Sodium Halides as a Source of Electrophilic Halogens

机译:卤化钠作为亲电卤素的绿色合成卤代噻吩硒基硒和苯并b硒代苯

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摘要

Herein, we report the first synthesis of chlorinated benzo[b]selenophenes via environmentally friendly electrophilic chlorocyclization reaction using “table salt” as a source of “electrophilic chlorine” and ethanol as a solvent. In addition, the synthesis of diverse halogenated heterocycles, including 3-chloro, 3-bromo and 3-iodo thiophenes, selenophenes, and benzo[b]selenophenes was successfully accomplished under the same environmentally benign reaction conditions. This methodology has several advantages over other previously reported reactions as it employs simple starting compounds, an environmentally friendly solvent, ethanol, and non-toxic inorganic reagents under mild reaction conditions, resulting in the high product yields.
机译:在此,我们报道了使用“食盐”作为“亲电子氯”的来源,并使用乙醇作为溶剂,通过环保的亲电子氯环化反应,首次合成了氯化苯并[b]硒代苯。另外,在相同的环境良性反应条件下,成功地完成了各种卤代杂环的合成,包括3-氯,3-溴和3-碘代噻吩,硒烯和苯并[b]硒烯。与以前报道的其他反应相比,该方法具有多种优势,因为它在温和的反应条件下采用了简单的起始化合物,环保溶剂,乙醇和无毒的无机试剂,从而提高了产品收率。

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