Réaction #1789

ord-bc2379efbe054eccaf35ae30843004da

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ExtractionThe solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL)
  2. 2
    SéchageThe organic phase was dried with MgSO4
  3. 3
    Filtrationfiltered
  4. 4
    Autrethe solvent removed under reduced pressure
  5. 5
    AutreThe residue was chromatographed on silica gel
  6. 6
    LavageMeOH and eluted with same
  7. 7
    Autrethe solvent was removed under reduced pressure the

Mode opératoire

The 2,4-dimethyl-3-chloromethylpyridine (21.5 g, 138 mmol) was dissolved in CHCl3 (800 mL) and cooled under nitrogen to 0° C. and m-chloroperbenzoic acid (55%, 35 g) was added in small portions. The reaction was stirred for 4 hours. The solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL). The organic phase was dried with MgSO4, filtered and the solvent removed under reduced pressure. The residue was chromatographed on silica gel packed in 98:2 CH2 Cl2 :MeOH and eluted with same. The appropriate fractions were combined and the solvent was removed under reduced pressure the give the desired 2,4-dimethyl-3-chloromethylpyridine-N-oxide.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05726172uspto-grants-1998_03