Реакция #55540

ord-2a046e2782934a18a6d5fb33db9480ed

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияthe solution was extracted with diethyl ether twice
  2. 2
    ПромывкаThe extract was washed with a saturated aqueous solution of sodium chloride
  3. 3
    Сушкаdried over magnesium sulfate
  4. 4
    КонцентрированиеThe solution was concentrated in vacuo
  5. 5
    Другоеthe residue was triturated with a solution of n-hexane and diethyl ether
  6. 6
    ФильтрацияThe precipitates were collected by filtration

Методика

Allyl bromide (2.91 g) was added dropwise to a stirred suspension of ethyl 2-(2-tritylaminothiazol-4-yl)-2-hydroxyiminoacetate (syn isomer, 10 g), N,N-dimethylformamide (100 ml) and potassium carbonate (4.54 g) under ice cooling over 5 minutes, and stirred at the same temperature for 4 hours. After adding water (200 ml) to the resultant solution, the solution was extracted with diethyl ether twice. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solution was concentrated in vacuo, and the residue was triturated with a solution of n-hexane and diethyl ether. The precipitates were collected by filtration to give ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 9.4 g), mp. 130° to 132° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04220761uspto-grants-1980_09