首页> 外文期刊>Monatshefte fur Chemie >Base-free benzylation of 1,3-dicarbonyl compounds using sulfamic acid supported on silica by linker: a combined experimental and theoretical approach
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Base-free benzylation of 1,3-dicarbonyl compounds using sulfamic acid supported on silica by linker: a combined experimental and theoretical approach

机译:1,3-二羰基化合物的无基苄基化合物使用连接物在二氧化硅上负载的氨基磺酸:一种综合的实验和理论方法

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摘要

Sulfamic acid stabilized on the surface of silica by the n-propyl organic group linker which is named silica-bonded N-propylsulfamic acid was applied as an efficient heterogeneous catalyst with good recyclability and reusability for direct benzylation of 1,3-dicarbonyl compounds using secondary aromatic alcohols or styrenes as alkylating agents in high yields and short reaction times. All the reactions were carried out in nitromethane as solvent under an air atmosphere. The catalyst showed reusable feature by six times without a significant loss in its activity.
机译:通过N-丙基有机群接头稳定在二氧化硅表面上稳定的氨基磺酸,其被命名为二氧化硅键合的正丙酸酸,作为有效的非均相催化剂,具有良好的再循环性和使用中学的1,3-二羰基化合物的直接苄基化的可重用性 芳香族醇或苯乙烯作为高产率和短反应时间的烷基化剂。 所有反应在硝基甲烷中在空气气氛下作为溶剂进行。 催化剂在其活动中显示可重复使用的特征,而没有显着损失。

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