Реакция #214768

ord-2f64fd19d21947a0b715b1e90e45cedb

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONare added
  2. 2
    ТемператураThe mixture is warmed on the steam cone until dissolution
  3. 3
    ДругоеIt is evaporated on the steam cone
  4. 4
    workup.ADDITIONthe solution poured into the mixture of 8 ml of 5 N hydrochloric acid and 300 ml of water
  5. 5
    ДругоеThe precipitated crystals are collected
  6. 6
    Промывкаwashed with water
  7. 7
    Другоеdried
  8. 8
    Другоеtriturated with methanol

Методика

To the suspension of 4.0 g of 1-methyl-β-oxo-2-pyrrolpropionitrile in 70 ml of toluene and 3.2 g of triethylamine, 3.7 g of p-fluorophenylisocyanate are added while stirring. The mixture is warmed on the steam cone until dissolution and the red-brown solution is allowed to stand overnight at room temperature. It is evaporated on the steam cone, the residue taken up in methanol and the solution poured into the mixture of 8 ml of 5 N hydrochloric acid and 300 ml of water. The precipitated crystals are collected, washed with water, dried, triturated with methanol and recrystalllized from ethyl acetate, to yield the 1-methyl-β-oxo-α-(p-fluorophenylcarbamoyl)-2-pyrrolpropionitrile melting at 198°-199°.

Источник

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