Reacción #214777
ord-7f0cfd9d05ac4a73ac9ff2e3359f2399
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroevaporated
- 2workup.DISSOLUTIONthe residue dissolved in methanol
- 3workup.ADDITIONThe solution is poured into 300 ml of water containing 5 ml of 5 N hydrochloric acid
- 4Otrothe precipitate is collected
- 5workup.DISSOLUTIONIt is dissolved in 5% aqueous sodium hydroxide
- 6Filtraciónthe solution filtered
- 7Otrothe filtrate re-acidified, the solids collected
- 8Lavadowashed with water
- 9Otrodried
- 10Otrorecrystallized from ethanol
Procedimiento
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°.