反应 #1973907

ord-c3aab4d8f0b246cab0e151da72871a66

反应方程式

O=C(Cl)COCc1ccccc1
Benzyloxy acetyl chloride
O=C(Cl)COCc1ccccc1
Benzyloxy Acetyl Chloride
COc1ccc(Cl)c(N)c1.Cl
2-chloro-5-methoxyaniline hydrochloride
CCN(CC)CC
triethylamine
COc1ccc(Cl)c(NC(=O)COCc2ccccc2)c1
2-Benzyloxy-N-(2-chloro-5-methoxy-phenyl) acetamide
收率 103.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The stirred reaction
  2. 2
    其他a heavy precipitation of triethylamine hydrochloride
  3. 3
    洗涤The dichloromethane solution was washed with 10% aqueous potassium carbonate (50 mL)
  4. 4
    干燥dried over magnesium sulfate
  5. 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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08501153B2uspto-grants-2013_08