反应 #302857

ord-0fda36c95d0a4a968ebfdb678629eeee

反应方程式

COc1ccc(O)c(C(C)=O)c1
5′-methoxy-2′-hydroxyacetophenone
O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
Cl
hydrochloric acid
COc1ccc(OC(=O)c2ccc([N+](=O)[O-])cc2)c(C(C)=O)c1
compound 21
COc1ccc(OC(=O)c2ccc([N+](=O)[O-])cc2)c(C(C)=O)c1
4-nitrobenzoic acid 2-acetyl-4-methoxyphenyl ester

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The obtained mixture was reacted at room temperature for 30 minutes
  2. 2
    温度under cooling on ice
  3. 3
    过滤The obtained precipitate was collected by filtration
  4. 4
    洗涤the filtrate was then washed with purified water

实验过程

5′-methoxy-2′-hydroxyacetophenone (1.5 g, 9.03 mmol) was added to a pyridine solution (20 ml) that contained 4-nitrobenzoyl chloride (1.72 g, 9.26 mmol) in an ice bath. The obtained mixture was reacted at room temperature for 30 minutes, and the reaction solution was then poured into 1 N hydrochloric acid under cooling on ice. The obtained mixture was intensively stirred. The obtained precipitate was collected by filtration, and the filtrate was then washed with purified water, so as to obtain a product of interest, 4-nitrobenzoic acid 2-acetyl-4-methoxyphenyl ester (compound 21). Yield: 2.49 g (yield constant: 87.4%)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08192717B2uspto-grants-2012_06