Reaktion #95076
ord-3857bd8cf78a4782ba6b7bc50758fb4c
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturThe mixture was heated
- 2Temperaturunder reflux for 10 minutes
- 3TemperaturThe mixture was again heated
- 4Temperaturunder reflux for 10 minutes
- 5TemperaturThe mixture was heated
- 6Temperaturunder reflux for 15 minutes
- 7SonstigeThe solvent was removed by evaporation in vacuo
- 8workup.DISSOLUTIONthe residue was dissolved in 75 ml
- 9WaschenThe ethyl acetate solution was washed successively with water, 1 N sodium hydroxide, water and saturated sodium chloride solution
- 10TrocknenThe ethyl acetate solution was then dried
- 11Sonstigethe ethyl acetate was removed by evaporation in vacuo
- 12SonstigeThe residue (960 mg.) was recrystallized from isopropyl ether giving 570 mg
Vorschrift
To a stirred solution of 829 mg. of N-decyl-3-(3-[4-carboxy-2-oxo-pyrrolidino]phenyl)propenamide in 25 ml. of tetrahydrofuran was added 357 mg. of carbonyldiimidazole. The mixture was heated under reflux for 10 minutes, and then 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was again heated under reflux for 10 minutes, and then an additional 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was heated under reflux for 15 minutes and then it was cooled to room temperature. The solvent was removed by evaporation in vacuo, and the residue was dissolved in 75 ml. of ethyl acetate. The ethyl acetate solution was washed successively with water, 1 N sodium hydroxide, water and saturated sodium chloride solution. The ethyl acetate solution was then dried using sodium sulfate, and the ethyl acetate was removed by evaporation in vacuo. The residue (960 mg.) was recrystallized from isopropyl ether giving 570 mg. of the title compound, m.p. 78°-80° C.