Reacción #2146704

ord-df12d0973c42432f9218ffc903decdb4

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 30 minutes
  2. 2
    workup.STIRRINGthe mixture was stirred for 1.5 hours
  3. 3
    TemperaturaAfter the reaction solution was cooled down
  4. 4
    workup.ADDITIONthe reaction solution was poured little by little
  5. 5
    Otroonto crushed ice
  6. 6
    Otroto generate precipitates
  7. 7
    FiltraciónThe precipitates were filtered
  8. 8
    Lavadowashed with water
  9. 9
    OtroThe precipitates obtained
  10. 10
    Secadowas dried over phosphorus pentaoxide under reduced pressure

Procedimiento

262 mL of conc. sulfuric acid was cooled down to −2° C., and 262 mL of 90% nitric acid was carefully added thereto. Then, 65.3 g (corresponding to 0.347 mmol) of 2-bromo-3-methoxypyridine was carefully thereto. After the resulting mixture was stirred in an ice bath for 10 minutes, the mixture was stirred at room temperature for 30 minutes. Then, after the temperature of the mixture was raised up to 55° C., the mixture was stirred for 1.5 hours. After the reaction solution was cooled down, the reaction solution was poured little by little onto crushed ice to generate precipitates. The precipitates were filtered and washed with water. The precipitates obtained was dried over phosphorus pentaoxide under reduced pressure to obtain 55.7 g (corresponding to 0.239 mol) of 2-bromo-3-methoxy-6-nitropyridine (FIG. 1, Step 2).

Fuente

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