Ammonium tetrafluoroborate: Novel Unprecedented Catalyst for the Synthesis of 3,4-dihydropyrimidin-2(1H)-ones through Biginelli Reaction

被引:0
|
作者
Verma, Aman [1 ]
Chaudhary, Gyanendra [1 ]
Verma, Deepti [1 ]
Prabhakar, Amit [2 ]
Behera, Kamalakanta [1 ]
机构
[1] Univ Allahabad, Dept Chem, Prayagraj, India
[2] Indian Inst Informat Technol Allahabad, Dept Appl Sci, Allahabad 211012, India
来源
CHEMISTRYSELECT | 2024年 / 9卷 / 08期
关键词
Biginelli reaction; 3,4-dihydropyrimidin-2(1H)-ones; ammonium tetrafluoroborate; catalyst; heterocycles; ONE-POT SYNTHESIS; ACIDIC IONIC LIQUID; SOLVENT-FREE; PROPARGYLIC ALCOHOLS; EFFICIENT CATALYST; HIGHLY EFFICIENT; SULFONIC-ACID; DIHYDROPYRIMIDINONES; ASSOCIATION; INHIBITORS;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel method has been developed to use ammonium tetrafluoroborate (NH4BF4) directly as catalyst in Biginelli reaction. A new paradigm of the Biginelli reaction for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones derivatives found the use of ammonium tetrafluoroborate as a novel, inexpensive, readily available, non-toxic and mild catalyst in good to excellent yields. Notably, this is the first time that ammonium tetrafluoroborate is directly used as a catalyst in organic synthesis. So far, no organic reaction is available in literature where NH4BF4 is directly used as catalyst. However, some reactions are found where NH4BF4 is used with other catalysts as promoters or additives. The protocol developed has several advantages, such as highly efficient, simple, atom-economical, environmentally friendly, easy synthetic and purification methods.
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页数:9
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