Réaction #2146704

ord-df12d0973c42432f9218ffc903decdb4

Équation de réaction

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

Conditions de réaction

Température
55°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  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
    TempératureAfter the reaction solution was cooled down
  4. 4
    workup.ADDITIONthe reaction solution was poured little by little
  5. 5
    Autreonto crushed ice
  6. 6
    Autreto generate precipitates
  7. 7
    FiltrationThe precipitates were filtered
  8. 8
    Lavagewashed with water
  9. 9
    AutreThe precipitates obtained
  10. 10
    Séchagewas dried over phosphorus pentaoxide under reduced pressure

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08277777B2uspto-grants-2012_10