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首页> 外文期刊>Synthetic Communications >Synthesis of a novel tetracationic acidic organic salt based on DABCO and its applications as catalyst in the Knoevenagel condensation reactions in water
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Synthesis of a novel tetracationic acidic organic salt based on DABCO and its applications as catalyst in the Knoevenagel condensation reactions in water

机译:基于DABCO的新型曲邻酸性有机盐及其应用在水中Knoevenagel缩合反应中的催化剂

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摘要

Synthesis of a novel tetracationic acidic organic salt based on DABCO containing two sulfonic acid groups in the skeleton and four hydrogensulfate groups as counterion is described. Its catalytic efficiency in the Knoevenagel condensation of aldehydes with active cyclic methylene compounds in water is investigated. While 2,2'-(phenylmethylene) bis(3-hydroxy-5,5-dimethylcyclohex-2-enone) derivatives were obtained in 40-98% isolated yields in the reaction of aldehydes with dimedone, the corresponding Knoevenagel adducts were provided in 85-95% yields using 1,3-dimethylbarbituric acid. In addition, a DABCO-based polycationic organic salt polymer was prepared and characterized for the first time.
机译:描述了一种基于骨骼中含有两种磺酸基团的Dabco的新酸性酸性有机盐作为骨架和四个氢磺酸盐基团作为抗衡离子。 研究其具有在水中有活性环状亚甲基化合物的醛肾上腺凝胶缩合的催化效率。 虽然2,2' - (苯基甲基)双(3-羟基-5,5-二甲基环己-2-烯酮)衍生物在40-98%的醛与DimEdode的反应中分离出来,但提供了相应的knoevenagel加合物 使用1,3-二甲基巴比妥酸的85-95%产率。 此外,制备了一种基于DABCO的聚阳离子有机盐聚合物并首次表征。

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