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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >Synthesis of 2-arylbenzothiazoles from 2-aminobenzenethiol and aryl aldehydes catalyzed by scandium triflate~1
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Synthesis of 2-arylbenzothiazoles from 2-aminobenzenethiol and aryl aldehydes catalyzed by scandium triflate~1

机译:三氟甲磺酸scan〜1催化2-氨基苯硫醇和芳醛合成2-芳基苯并噻唑

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摘要

2-Aminobenzenethiol and an aryl aldehyde reactded to give a benzothiazoline via an imine intermediate,and the benzothiazoline was aromatized by oxygen or hydrogen peroxide to give a high yield of 2-arylbenzothiazole in the presence of a catalytic amount of scanding triflate Sc(OtF)_3.The intermediary benzothiazoline was isolated adn allowed to react wtih O_2 or H_2O_2 in the presence of Sc(OTf)_3,and the lewis acid was found to also catalyze the oxidative process other than the ring closing step.
机译:2-氨基苯硫酚与芳基醛通过亚胺中间体反应生成苯并噻唑啉,并在催化量的三氟甲磺酸Sc Sc(OtF)存在下,用氧气或过氧化氢将苯并噻唑啉芳构化,以高产率得到2-芳基苯并噻唑_3。在Sc(OTf)_3存在下,分离中间体苯并噻唑啉并使其与O_2或H_2O_2反应,发现路易斯酸除了闭环步骤外还催化氧化过程。

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