反应 #710464
ord-8b9176addbc149a8a16572577beef07f
反应方程式
反应条件
后处理
- 1workup.STIRRINGthe mixture was stirred for 10 minutes
- 2其他The mixture was transferred to a separatory funnel
- 3其他liquid separation
- 4洗涤the organic layer was washed twice with 150 ml of water and twice with 150 ml of a 1% HCl aqueous solution
- 5干燥dried over anhydrous magnesium sulfate
- 6浓缩concentrated under reduced pressure
实验过程
25 g (270 mmol) of 2-aminopyridine was dissolved in 200 ml of anhydrous dichloromethane, 41 ml (30 g, 300 mmol) of triethylamine was added thereto, and the mixture was cooled to 0° C. 38 ml (57 g, 270 mmol) of anhydrous trifluoroacetic acid was added dropwise thereto over 15 minutes, and the resulting mixture was stirred at room temperature for 2 hours. After the reaction was completed, the reaction solution was injected into about 100 ml of iced water, and the mixture was stirred for 10 minutes. The mixture was transferred to a separatory funnel to perform liquid separation, and the organic layer was washed twice with 150 ml of water and twice with 150 ml of a 1% HCl aqueous solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 36 g (yield 71%) of 2,2,2-trifluoro-N-(pyridin-2(1H)-ylidene)acetamide.