40736-25-2Relevant articles and documents
Method for catalytically synthesizing acrylamide compound by MOFs-derived zirconium-based ternary oxide solid acid
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Paragraph 0073-0074, (2021/11/14)
The invention provides a catalytic synthesis of acrylamide compounds with zirconium-based ternary oxide solid acid as a catalyst, and the low-temperature activity is good. In the synthesis process, the acid is small, the reaction conditions are mild and controllable, the byproducts are few, the reaction yield is effectively improved, the purity is high, the quality is good, and the method is suitable for large-scale production.
Aza-Michael addition of aliphatic or aromatic amines to α,β-unsaturated compounds catalyzed by a DBU-derived ionic liquid under solvent-free conditions
Ying, An-Guo,Liu, Luo,Wu, Guo-Feng,Chen, Gang,Chen, Xin-Zhi,Ye, Wei-Dong
body text, p. 1653 - 1657 (2009/06/28)
A task-specific ionic liquid, 1,8-diazabicyclo[5.4.0]-undec-7-en-8-ium acetate has been successfully used as a catalyst for aza-conjugate addition of aliphatic or aromatic amines to various electron deficient alkenes under solvent-free conditions and at room temperature. The catalyst can be reused for six times without noticeable loss of activity.
ANNULATION OF IMIDAZOLINES: SYNTHESIS OF IMIDAZOPYRIDONES
Jones, Raymond C. F.,Smallridge, Mark J.
, p. 5005 - 5008 (2007/10/02)
The enaminoester 1-benzyl-2-(ethoxycarbonylmethylene)-imidazolidine undergoes N-acylation and conjugate C-addition with α,β-unsaturated acyl imidazolides to afford imidazopyridones.