首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of 4H-Benzopyrans Catalyzed by Acyclic Acidic Ionic Liquids tin Aqueous Media
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Synthesis of 4H-Benzopyrans Catalyzed by Acyclic Acidic Ionic Liquids tin Aqueous Media

机译:无环酸性离子液体锡水性介质催化合成4H-苯并吡喃

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摘要

Some halogen-free acyclic task-specific ionic liquids (TSILs) were synthesized as novel and recyclable catalysts for the synthesis of 5-oxo-5,6,7,8-tetrahydi-o-4H-benzo[b]pyrans by one-pot three-component condensation of aromatic aldehyde, malononitrile (or ethyl cyanoacetate), and dimedone (or 1,3-cyclohexanedione) in water. The condensation accomplished successfully with good yields ranged from 86 to 94%. After the reaction, the products could simply be separated from the catalyst/water, and the catalyst could be reused at least 10 times without noticeably decreasing the catalytic activity.
机译:合成了一些无卤的无环非离子型特定任务离子液体(TSIL),将其作为一种新型可循环使用的催化剂,用于通过一种方法合成5-oxo-5,6,7,8-四氢-邻-4H-苯并[b]吡喃。将芳族醛,丙二腈(或氰基乙酸乙酯)和二甲酮(或1,3-环己二酮)在水中进行三组分缩合。缩合成功完成,收率在86%至94%之间。反应后,可以简单地将产物与催化剂/水分离,并且催化剂可以重复使用至少10次,而不会明显降低催化活性。

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