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无催化剂条件下有效的四组分反应合成2,3-二氢噻吩衍生物 被引量:1

An Efficient Synthesis of 2,3-Dihydrothiophene Derivatives from Four-Component Reactions under Catalyst-Free Conditions
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摘要 芳香醛、2,4-噻唑烷二酮、丙二腈和3-吡啶甲胺于95%乙醇中四组分反应,方便地获得一系列新的2,3-二氢噻吩衍生物.这是杂环胺类化合物首次应用于噻吩衍生物的合成,具有反应条件温和、容易操作、产率高等优点.产物的结构经过红外、核磁和高分辨质谱确定. An efficient synthesis of 2,3-dihydrothiophene derivatives by the four-component reactions of aromatic aldehydes, thiazolidine-2,4-dione, malononitrile and pyridin-3-ylmethanamine has been reported. This reaction could be carried out smoothly without using any other catalysts in ethanol (95%) and the aromatic heterocyclic amine (pyridin-3-ylmethanamine) was first used for the synthesis of 2,3-dihydrothiophene derivatives. The advantages of this procure were mild reaction condi- tions, easy operation, and high yields. The products were identified by IR, XH NMR and HRMS.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2014年第9期1895-1899,共5页 Chinese Journal of Organic Chemistry
基金 国家自然科学基础研究基金(No.21172188) 江苏省功能性材料绿色合成重点实验室开放课题(No.K201312)资助项目~~
关键词 噻吩 2 4-噻唑烷二酮 3-吡啶甲胺 四组分反应 thiophene thiazolidine-2,4-dione pyridin-3-ylmethanamine four-component reactions
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