反应 #417964

ord-b36c980b138d4933833e7cd7a8fdd153

反应方程式

CC(=O)OC(C)=O
Acetic anhydride
Nc1ccc(Cl)c(O)c1
4-chloro-3-hydroxy aniline
CC(=O)Nc1ccc(Cl)c(O)c1
product 17a
收率 93.0%
CC(=O)Nc1ccc(Cl)c(O)c1
N-(4-chloro-3-hydroxyphenyl)acetamide
收率 93.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the reaction was refluxed for 5 mins
  2. 2
    过滤It was filtered off
  3. 3
    洗涤washed with water (10 mL)
  4. 4
    其他dried

实验过程

Acetic anhydride (3.0 mL, 42.0 mmol) was added to a solution of 4-chloro-3-hydroxy aniline (4.0 g, 28 mmol) in acetic acid (20 mL), and the reaction was refluxed for 5 mins. The reaction mixture was cooled to room temperature and the product was solidified. It was filtered off and washed with water (10 mL) and dried to obtain the product 17a in 93% yield (4.8 g) as a creamy white solid. There was no need for further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08877752B2uspto-grants-2014_11