New method for preparing double-(hetero)aromatic-ring substituted alkene
A new method and aromatic technology, which is applied in the preparation of carboxylic acid nitriles, chemical instruments and methods, and the preparation of organic compounds. It can solve the problems of a large number of catalysts, harsh reaction conditions, catalyst recovery and mechanical application, and large-scale promotion and use.
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Embodiment 1
[0024] Thiphenaldehyde (5mmol), 2-cyanomethylbenzimidazole (5mmol), 0.735g catalyst, and water (10mL) were sequentially added into a 50mL three-neck flask, stirred at room temperature for 2 hours, and detected by TLC, the raw materials basically disappeared. The catalyst was collected, the reaction solution was poured out, filtered, and the obtained solid was recrystallized with ethanol to obtain the product with a yield of 79% and a content of 98%.
[0025] 2-(1H-benzoimidazol-2-yl)-3-(thiophen-2-yl)acrylonitrile: 1 H NMR (400MHz, CDCl 3 ):δ7.15-7.22(m,1H),7.30-7.37(m,2H),7.50-7.52(m,1H),7.66-7.70(m,2H),7.76-7.77(m,1H),7.87 -7.89(m,1H),8.63(s,1H); 13 C NMR (100MHz, CDCl 3 ): δ98.1, 115.6, 115.7, 116.7, 123.6, 129.1, 134.5, 136.8, 137.0, 139.3, 147.6.
Embodiment 2
[0027] Thiphenaldehyde (5mmol), 2-cyanomethylbenzimidazole (5mmol), 0.147g catalyst, and water (10mL) were sequentially added into a 50mL three-neck flask, stirred at room temperature for 5 hours, and detected by TLC, the raw materials basically disappeared, and an external magnetic field was applied to absorb The catalyst was collected, the reaction solution was poured out, filtered, and the obtained solid was recrystallized with ethanol to obtain the product with a yield of 62% and a content of 97%.
Embodiment 3
[0029] Thiphenaldehyde (5mmol), 2-cyanomethylbenzimidazole (6mmol), 0.147g catalyst, and water (10mL) were sequentially added into a 50mL three-neck flask, stirred at room temperature for 3 hours, and detected by TLC, the raw materials basically disappeared, and an external magnetic field was applied to absorb The catalyst was collected, the reaction solution was poured out, filtered, and the obtained solid was recrystallized with ethanol to obtain the product with a yield of 76% and a content of 99%.
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