Reacción #50547

ord-e47ac9fd260047e6b8625e28c037e1c0

Ecuación de reacción

Oc1cccc(Br)c1
3-Bromophenol
CCN(CC)CC
triethylamine
CC(=O)Cl
Acetyl chloride
CC(=O)Oc1cccc(Br)c1
3-bromophenyl acetate
Rendimiento 99.4%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe solution was cooled in an ice bath
  2. 2
    OtroAfter 1 h the cooling bath was removed
  3. 3
    LavadoThe mixture was washed with hydrochloric acid (1N, 250 mL), water (250 mL), 5% NaHCO3 (250 mL), and brine (250 mL)
  4. 4
    OtroThe organic layer was dried
  5. 5
    Otroevaporated

Procedimiento

3-Bromophenol (100 g, 580 mmol) and triethylamine (104 mL, 750 mmol) were dissolved in dichloromethane (500 mL), and the solution was cooled in an ice bath. Acetyl chloride (49.7 g, 630 mmol) was added dropwise. After 1 h the cooling bath was removed and the mixture was stirred overnight (approx 16 h) at room temperature. The mixture was washed with hydrochloric acid (1N, 250 mL), water (250 mL), 5% NaHCO3 (250 mL), and brine (250 mL). The organic layer was dried and evaporated to provide 124 g (99%) of 3-bromophenyl acetate as a light brown liquid; 1H NMR (CDCl3) δ7.36 (d, 1H), 7.32-7.20 (m, 2H), 7.05 (d, 1H), 2.28 (s, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05428040uspto-grants-1995_06