Reacción #5608
ord-5543a960e72d4b11830530e7308453a5
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Concentraciónthe mixture was concentrated under reduced pressure to dryness
- 2workup.DISSOLUTIONThe residue was dissolved in methanol
- 3Filtraciónthe insoluble material was filtered off
- 4OtroThe filtrate was evaporated in vacuo
Procedimiento
To a mixture of 2-chloromethyl-5-benzyloxy-4-pyridone (1.0 g), tetrahydrofuran (10 ml) and water (10 ml) were added dimethylamine hydrochloride (1.31 g) and sodium hydroxide (0.64 g). After being stirred for 1.5 hours, the mixture was concentrated under reduced pressure to dryness. The residue was dissolved in methanol and the insoluble material was filtered off. The filtrate was evaporated in vacuo to give 5-benzyloxy-2-(N,N-dimethylamino)methyl-4-pyridone (1.0 g) as a powder.