Reacción #162817
ord-5bc2ea202f5a4324ab8f4d8de557b541
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.ADDITIONwas added under a nitrogen atmosphere
- 2workup.STIRRINGThe mixture was stirred at 100° C. for 1.5 hrs
- 3Temperaturato cool to room temperature
- 4ConcentraciónThe reaction mixture was concentrated under reduced pressure
- 5workup.ADDITIONEthanol (500 ml) was added to the residue
- 6workup.STIRRINGthe mixture was stirred at 90° C
- 7TemperaturaWhen the mixture was cooled to 40° C.
- 8Filtraciónthe crystals were collected by filtration
- 9Lavadowashed with ethanol
- 10Otrodried
Procedimiento
Acetic anhydride (290 ml) was added to 1,3-diphenylurea 18 (148 g), malonic acid 4 (81.6 g) was added under a nitrogen atmosphere, and the mixture was stirred at 90° C. for 3 hrs. The mixture was stirred at 100° C. for 1.5 hrs and allowed to cool to room temperature. The reaction mixture was concentrated under reduced pressure. Ethanol (500 ml) was added to the residue, and the mixture was stirred at 90° C. When the mixture was cooled to 40° C., the crystals were collected by filtration, washed with ethanol and dried to give 1,3-diphenyl-pyrimidine-2,4,6-trione 19 (78.0 g, yield 40%).