Reacción #1789
ord-bc2379efbe054eccaf35ae30843004da
Ecuación de reacción
2,4-dimethyl-3-chloromethylpyridine
m-chloroperbenzoic acid
→
2,4-dimethyl-3-chloromethylpyridine-N-oxide
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ExtracciónThe solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL)
- 2SecadoThe organic phase was dried with MgSO4
- 3Filtraciónfiltered
- 4Otrothe solvent removed under reduced pressure
- 5OtroThe residue was chromatographed on silica gel
- 6LavadoMeOH and eluted with same
- 7Otrothe solvent was removed under reduced pressure the
Procedimiento
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.