Reacción #214768

ord-2f64fd19d21947a0b715b1e90e45cedb

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONare added
  2. 2
    TemperaturaThe mixture is warmed on the steam cone until dissolution
  3. 3
    OtroIt 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
    OtroThe precipitated crystals are collected
  6. 6
    Lavadowashed with water
  7. 7
    Otrodried
  8. 8
    Otrotriturated with methanol

Procedimiento

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°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04256759uspto-grants-1981_03