Reacción #48099

ord-d7be8da01baa476ab577c06803cac38a

Disolventes

Condiciones de reacción

Temperatura
-5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónfiltered
  2. 2
    Otroseparated from all volatile constituents in a rotary evaporator
  3. 3
    workup.DISSOLUTIONThe residue is dissolved in 150 mL dichloromethane
  4. 4
    workup.ADDITION46.5 g anisole are added
  5. 5
    workup.ADDITIONThen 51.5 g aluminum trichloride are added batchwise so that the temperature
  6. 6
    Otrodoes not exceed 5° C
  7. 7
    workup.STIRRINGThe solution is stirred for 1 h at 1 to 5° C.
  8. 8
    workup.ADDITIONpoured
  9. 9
    Otroonto crushed ice
  10. 10
    OtroThe organic phase is separated off
  11. 11
    Extracciónthe aqueous phase is extracted with dichloromethane
  12. 12
    LavadoThe combined organic phases are washed with 1 M hydrochloric acid, twice with 1 M sodium hydroxide solution and with brine
  13. 13
    SecadoThen the organic phase is dried over sodium sulfate
  14. 14
    Otrothe solvent is removed
  15. 15
    Otrothe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745414B2uspto-grants-2010_06