反应 #1973907
ord-c3aab4d8f0b246cab0e151da72871a66
反应方程式
反应物
试剂
反应条件
后处理
- 1其他The stirred reaction
- 2其他a heavy precipitation of triethylamine hydrochloride
- 3洗涤The dichloromethane solution was washed with 10% aqueous potassium carbonate (50 mL)
- 4干燥dried over magnesium sulfate
- 5浓缩concentrated in vacuo
实验过程
Benzyloxy acetyl chloride (1) (11.0 g, 60.0 mmol) and 2-chloro-5-methoxyaniline hydrochloride (11.7 g, 60.2 mmol) in dichloromethane (100 mL) at 0° C., was stirred and triethylamine (13.0 g 126.0 mmol, 18.0 mL) added slowly over 15 min. The stirred reaction was allowed to warm to RT over 18 h. There was a heavy precipitation of triethylamine hydrochloride. The dichloromethane solution was washed with 10% aqueous potassium carbonate (50 mL), dried over magnesium sulfate and concentrated in vacuo to afford 18.9 g (quantitative) of 2-Benzyloxy-N-(2-chloro-5-methoxy-phenyl) acetamide (2) as a gum. The structure was confirmed by 13C NMR (75 MHz, CDCl3): δC 55.6, 69.6, 73.6, 106.2, 111.1, 114.1, 127.7, 128.3, 128.6, 129.2, 134.6, 136.5, 158.9, and 167.7.