Reacción #362829
ord-4abb63068c0a4f0a818134184308a10e
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturawhich is maintained under nitrogen
- 2Temperaturacooled down
- 3Extracciónextracted with 100 ml of dichloromethane and 100 ml of distilled water
- 4OtroThe aqueous phase is separated off
- 5Lavadowashed with 3 times 100 ml of dichloromethane
- 6Lavadowashed with 100 ml of water
- 7Otrowith 100 ml of a saturated solution of NaCl, separated off
- 8Secadodried over magnesium sulphate
- 9Filtraciónthe phases are filtered
- 10Otroevaporated to dryness under reduced pressure (50 kPa) in order
Procedimiento
4,6 g of diethyl 4-aminobenzylacetamidomalonate in 104 ml of acetic acid are placed in a three-necked flask which is maintained under nitrogen. 7.02 g of sodium acetate are added, followed by 1.87 ml of 2,5-dimethoxytetrahydrofuran. The mixture is heated at 65° C. for 1 h 15 min, then cooled down and extracted with 100 ml of dichloromethane and 100 ml of distilled water. The aqueous phase is separated off after settling and then washed with 3 times 100 ml of dichloromethane. The organic phases are combined, washed with 100 ml of water and then with 100 ml of a saturated solution of NaCl, separated off after settling and then dried over magnesium sulphate; the phases are filtered and then evaporated to dryness under reduced pressure (50 kPa) in order to yield 6.2 g of a solid which is purified by flash chromatography (eluent CH2Cl2/acetone 75/25 by volume). This results in 3.57 g of diethyl 4-(1-pyrrolyl)benzylacetamidomalonate in the form of a beige solid which melts at 110° C.