Réaction #1789
ord-bc2379efbe054eccaf35ae30843004da
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1ExtractionThe solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL)
- 2SéchageThe organic phase was dried with MgSO4
- 3Filtrationfiltered
- 4Autrethe solvent removed under reduced pressure
- 5AutreThe residue was chromatographed on silica gel
- 6LavageMeOH and eluted with same
- 7Autrethe 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.