Реакция #214777

ord-7f0cfd9d05ac4a73ac9ff2e3359f2399

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеevaporated
  2. 2
    workup.DISSOLUTIONthe residue dissolved in methanol
  3. 3
    workup.ADDITIONThe solution is poured into 300 ml of water containing 5 ml of 5 N hydrochloric acid
  4. 4
    Другоеthe precipitate is collected
  5. 5
    workup.DISSOLUTIONIt is dissolved in 5% aqueous sodium hydroxide
  6. 6
    Фильтрацияthe solution filtered
  7. 7
    Другоеthe filtrate re-acidified, the solids collected
  8. 8
    Промывкаwashed with water
  9. 9
    Другоеdried
  10. 10
    Другоеrecrystallized from ethanol

Методика

The mixture of 2.1 g of 1-ethyl-β-oxo-2-pyrrolpropionitrile, 25 ml of toluene and 1.6 g of triethylamine is treated with 1.6 g of phenylisocyanate while stirring. It is allowed to stand overnight at room temperature, evaporated and the residue dissolved in methanol. The solution is poured into 300 ml of water containing 5 ml of 5 N hydrochloric acid and the precipitate is collected. It is dissolved in 5% aqueous sodium hydroxide, the solution filtered, the filtrate re-acidified, the solids collected, washed with water, dried and recrystallized from ethanol, to yield the 1-ethyl-β-oxo-α-phenylcarbamoyl-2-pyrrolpropionitrile melting at 144°-145°.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04256759uspto-grants-1981_03