Knoevenagel冷凝
化学
迈克尔反应
催化作用
离子液体
哌啶
有机化学
缩合反应
绿色化学
高分子化学
作者
Pengkun Yang,Yawei Liu,Ling Chai,Zhen‐Zhen Lai,Xiaomin Fang,Baoying Liu,Wenkai Zhang,Minghua Lu,Yuanqing Xu,Hao Xu
标识
DOI:10.1080/00397911.2018.1434544
摘要
A series of novel N-methyl piperidine (Nmp)-based ionic liquids with 1,2-propanediol group are synthesized and used as catalysts for both hetero-Michael addition of α,β-unsaturated amides and Knoevenagel condensation at room temperature in water; and all the examined substrates could be transformed into corresponding products in good to excellent yields. Meanwhile IL-catalyzed hetero-Michael addition of α,β-unsaturated amides in water has not been reported in the previous literatures. Additionally, the catalyst is recyclable for the two reactions. This finding provides a green catalyst for both hetero-Michael addition of α,β-unsaturated amides and Knoevenagel condensation in water.
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