Reacción #52992

ord-d19da1de04634b748ce0f22f3758a50c

Disolventes

Condiciones de reacción

Temperatura
2.5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe mixture was stirred for 30 min at that temperature
  2. 2
    workup.STIRRINGthe mixture was stirred for 30 min
  3. 3
    OtroThe resulting precipitate was collected
  4. 4
    Lavadowashed successively with cold water, MeOH and ether
  5. 5
    SecadoThe solid was then dried over conc. H2SO4 in a vacuum dessicator for a few days
  6. 6
    TemperaturaThe solid was heated with a bunsen burner until all the solid
  7. 7
    workup.DISTILLATIONThe resulting fumes were collected over water (distilling apparatus)
  8. 8
    OtroThe product was then recovered with Et2O
  9. 9
    OtroThe solvent was evaporated
  10. 10
    Otrothe crude product was purified by preparative TLC (silica gel; eluent: hexane/AcOEt 50:1 to 20:1)

Procedimiento

4-Amino-2,6-dichlorobenzoic acid methyl ester (0.5 g) was suspended in 15% HCl (10 mL) and stirred for 30 min then cooled to 0-5° C. After addition of NaNO2 (188 mg) in small portions, the mixture was stirred for 30 min at that temperature. Precooled HBF4 (0.46 mL) was added and the mixture was stirred for 30 min. The resulting precipitate was collected and washed successively with cold water, MeOH and ether. The solid was then dried over conc. H2SO4 in a vacuum dessicator for a few days. The solid was heated with a bunsen burner until all the solid has melted. The resulting fumes were collected over water (distilling apparatus). The product was then recovered with Et2O. The solvent was evaporated and the crude product was purified by preparative TLC (silica gel; eluent: hexane/AcOEt 50:1 to 20:1) to give 2,6-dichloro-4-fluorobenzoic acid methyl ester (241 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06855843B2uspto-grants-2005_02