反应 #75429

ord-2abe76b980254f9eb3d2fd29f5a44d81

反应方程式

Cc1cc(O)ccc1Cl
4-chloro-3-methylphenol
CC(=O)OC(C)=O
acetic anhydride
CC(=O)Oc1ccc(Cl)c(C)c1
4-Chloro-3-methylphenyl Acetate

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他equipped with a reflux condenser
  2. 2
    萃取The mixture was then extracted with 400 ml of diethyl ether
  3. 3
    干燥The organic phase was dried over magnesium sulfate
  4. 4
    workup.DISTILLATIONthe ether was distilled off
  5. 5
    workup.DISTILLATIONThe raw product is subsequently distilled under reduced pressure (b.p. 65-68° C., 20 mbar)

实验过程

43.0 g (0.30 mol) of 4-chloro-3-methylphenol, 34 ml (0.36 mol) of acetic anhydride and a few drops of concentrated sulfuric acid were stirred for 2 h at 60° C. in a 250 ml flask equipped with a reflux condenser. The reaction mixture was cooled to room temperature, poured into 200 ml of water and stirred for 1 h at room temperature. The mixture was then extracted with 400 ml of diethyl ether. The organic phase was dried over magnesium sulfate and the ether was distilled off. The raw product is subsequently distilled under reduced pressure (b.p. 65-68° C., 20 mbar).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06699405B2uspto-grants-2004_03