Реакция #4455

ord-c74194e3c47f4eb68794e86e6dfaa233

Растворители

Условия реакции

Температура
5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеEvaporation of the solvent
  2. 2
    Другоеgave a residue, which
  3. 3
    Экстракцияwas extracted with ethyl acetate (150 ml)
  4. 4
    ПромывкаThe extract was washed with water
  5. 5
    Сушкаdried over magnesium sulfate
  6. 6
    ДругоеThe solvent was evaporated in vacuo

Методика

To a solution of N-amino-1,2,3,6-tetrahydropyridine hydrochloride (1.346 g) and triethylami-ne (2.024 g) in methylene chloride (60 ml) was added a solution of phenyl chloroformate (1.566 g) in methylene chloride (40 ml) and the mixture was stirred for 4 hours at 5° C. Evaporation of the solvent gave a residue, which was extracted with ethyl acetate (150 ml). The extract was washed with water and dried over magnesium sulfate. The solvent was evaporated in vacuo to give N-(phenoxy- carbonylamino)-1,2,3,6-tetrahydropyridine (2.01 g), which was recrystallized from diisopropyl ether to give the desired compound (0.732 g) as colorless needles. mp: 124°-125.5° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725608uspto-grants-1988_02