Reacción #52992
ord-d19da1de04634b748ce0f22f3758a50c
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGthe mixture was stirred for 30 min at that temperature
- 2workup.STIRRINGthe mixture was stirred for 30 min
- 3OtroThe resulting precipitate was collected
- 4Lavadowashed successively with cold water, MeOH and ether
- 5SecadoThe solid was then dried over conc. H2SO4 in a vacuum dessicator for a few days
- 6TemperaturaThe solid was heated with a bunsen burner until all the solid
- 7workup.DISTILLATIONThe resulting fumes were collected over water (distilling apparatus)
- 8OtroThe product was then recovered with Et2O
- 9OtroThe solvent was evaporated
- 10Otrothe 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).