Reacción #48099
ord-d7be8da01baa476ab577c06803cac38a
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Filtraciónfiltered
- 2Otroseparated from all volatile constituents in a rotary evaporator
- 3workup.DISSOLUTIONThe residue is dissolved in 150 mL dichloromethane
- 4workup.ADDITION46.5 g anisole are added
- 5workup.ADDITIONThen 51.5 g aluminum trichloride are added batchwise so that the temperature
- 6Otrodoes not exceed 5° C
- 7workup.STIRRINGThe solution is stirred for 1 h at 1 to 5° C.
- 8workup.ADDITIONpoured
- 9Otroonto crushed ice
- 10OtroThe organic phase is separated off
- 11Extracciónthe aqueous phase is extracted with dichloromethane
- 12LavadoThe combined organic phases are washed with 1 M hydrochloric acid, twice with 1 M sodium hydroxide solution and with brine
- 13SecadoThen the organic phase is dried over sodium sulfate
- 14Otrothe solvent is removed
- 15Otrothe residue is recrystallized from ethanol
Procedimiento
38.3 mL oxalyl chloride and 0.8 mL dimethylformamide are added to a mixture of 100 g 5-bromo-2-chloro-benzoic acid in 500 mL dichloromethane. The reaction mixture is stirred for 14 h, then filtered and separated from all volatile constituents in a rotary evaporator. The residue is dissolved in 150 mL dichloromethane, the resultant solution is cooled to −5° C., and 46.5 g anisole are added. Then 51.5 g aluminum trichloride are added batchwise so that the temperature does not exceed 5° C. The solution is stirred for 1 h at 1 to 5° C. and then poured onto crushed ice. The organic phase is separated off, and the aqueous phase is extracted with dichloromethane. The combined organic phases are washed with 1 M hydrochloric acid, twice with 1 M sodium hydroxide solution and with brine. Then the organic phase is dried over sodium sulfate, the solvent is removed and the residue is recrystallized from ethanol.