Реакция #1788

ord-bfc9e545236f4da9864ea3f99c2d6fe8

Реагенты

Нет

Растворители

Условия реакции

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

Обработка

  1. 1
    ДругоеThe solvent was removed under reduced pressure
  2. 2
    Другоеthe residue was partitioned between CH2Cl2 and saturated aqueous sodium bicarbonate
  3. 3
    СушкаThe organic layer was dried with MgSO4
  4. 4
    Фильтрацияfiltered
  5. 5
    Другоеthe solvent removed under reduced pressure

Методика

The 2,4-dimethyl-3-hydroxymethylpyridine (19.2 g, 140 mmol) was dissolved in CH2Cl2 (800 mL) and cooled under nitrogen to 0° C. and thionyl chloride (125 mL) was slowly added and the reaction was stirred for 18 hours. The solvent was removed under reduced pressure and the residue was partitioned between CH2Cl2 and saturated aqueous sodium bicarbonate. The organic layer was dried with MgSO4, filtered and the solvent removed under reduced pressure to give the desired 2,4-dimethyl-3-chloromethylpyridine.

Источник

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