Реакция #1789

ord-bc2379efbe054eccaf35ae30843004da

Уравнение реакции

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

Реагенты

Нет

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ЭкстракцияThe solution was extracted twice with saturated aqueous sodium bicarbonate (500 mL)
  2. 2
    СушкаThe organic phase was dried with MgSO4
  3. 3
    Фильтрацияfiltered
  4. 4
    Другоеthe solvent removed under reduced pressure
  5. 5
    ДругоеThe residue was chromatographed on silica gel
  6. 6
    ПромывкаMeOH and eluted with same
  7. 7
    Другоеthe solvent was removed under reduced pressure the

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726172uspto-grants-1998_03