Reacción #2146689

ord-607571f9c2a748aca1fa898a338aef5f

Ecuación de reacción

O=S(=O)(O)O
sulfuric acid
O=[N+]([O-])O
nitric acid
COc1cccnc1Br
2-bromo-3-methoxypyridine
COc1ccc([N+](=O)[O-])nc1Br
2-bromo-3-methoxy-6-nitropyridine

Condiciones de reacción

Temperatura
55°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe mixture was stirred at room temperature for 10 minutes
  2. 2
    workup.STIRRINGfurther stirred for one hour
  3. 3
    TemperaturaAfter the reaction solution was cooled to room temperature
  4. 4
    workup.ADDITIONthe reaction solution was poured little by little
  5. 5
    Otrointo crushed ice
  6. 6
    Otroto generate precipitates
  7. 7
    FiltraciónThe precipitates were filtered
  8. 8
    Lavadowashed with water
  9. 9
    Secadodried over phosphorus pentaoxide under reduced pressure

Procedimiento

83 mL of conc. sulfuric acid was cooled down to −5° C., and 83 mL of 90% nitric acid was carefully added thereto. Subsequently, 20.69 g (corresponding to 110.04 mmol) of 2-bromo-3-methoxypyridine was carefully added thereto. After the reaction mixture was stirred in an ice bath for 5 minutes, the mixture was stirred at room temperature for 10 minutes, and then was heated to 55° C. and further stirred for one hour. After the reaction solution was cooled to room temperature, the reaction solution was poured little by little into crushed ice to generate precipitates. The precipitates were filtered and washed with water, and then dried over phosphorus pentaoxide under reduced pressure, to obtain 17.41 g (corresponding to 74.71 mmol) of 2-bromo-3-methoxy-6-nitropyridine (FIG. 3, Step 2).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08277777B2uspto-grants-2012_10