Reacción #75429

ord-2abe76b980254f9eb3d2fd29f5a44d81

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with a reflux condenser
  2. 2
    ExtracciónThe mixture was then extracted with 400 ml of diethyl ether
  3. 3
    SecadoThe 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)

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06699405B2uspto-grants-2004_03