Reacción #1099628
ord-74279030f34347c8b189d5d9dc1e5231
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.STIRRINGAfter stirring at room temperature for 2 hr
- 2Extracciónthe mixture was extracted with ethyl acetate
- 3LavadoThe obtained organic layer was washed with saturated brine
- 4Secadodried over anhydrous magnesium sulfate
- 5Concentraciónconcentrated under reduced pressure
Procedimiento
To a solution of 1-(2,6-difluorophenyl)ethanone (10.0 g) in diethyl ether (50 mL) was added anhydrous aluminum chloride (86 mg) and the mixture was stirred for 5 min. Bromine (3.3 mL) was added dropwise at 10-15° C. After stirring at room temperature for 2 hr, the mixture was poured into water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, concentrated under reduced pressure to give the title compound as a pale-yellow oil (yield 15.2 g, about 100%).