Reacción #1789

ord-bc2379efbe054eccaf35ae30843004da

Ecuación de reacción

Cc1ccnc(C)c1CCl
2,4-dimethyl-3-chloromethylpyridine
O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
Cc1cc[n+]([O-])c(C)c1CCl
2,4-dimethyl-3-chloromethylpyridine-N-oxide

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL)
  2. 2
    SecadoThe organic phase was dried with MgSO4
  3. 3
    Filtraciónfiltered
  4. 4
    Otrothe solvent removed under reduced pressure
  5. 5
    OtroThe residue was chromatographed on silica gel
  6. 6
    LavadoMeOH and eluted with same
  7. 7
    Otrothe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726172uspto-grants-1998_03