Reacción #5610
ord-03e7daa11f954f73ad1160c376faaee0
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturawas heated
- 2Temperaturarefluxed for an hour
- 3TemperaturaThe mixture was cooled
- 4Filtraciónthe resulting precipitate was collected by filtration
- 5Lavadowashed with diisopropyl ether
- 6Otroair-dried at ambient temperature
Procedimiento
A mixture of 5-benzyloxy-2-vinyl-4-pyridone (2.90 g) and pyrrolidine (5.33 ml) was heated and refluxed for an hour. The mixture was cooled and diluted with tetrahydrofuran (20 ml) and diisopropyl ether (80 ml). After being stirred for an hour at ambient temperature, the resulting precipitate was collected by filtration, washed with diisopropyl ether and air-dried at ambient temperature to give 5-benzyloxy-2-[2-(1-pyrrolidinyl)ethyl]4-pyridone (3.79 g).