Reacción #736393
ord-0833907527804ce6a54ae24e158f665d
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturathe solution was refluxed
- 2Temperaturaby heating for 10 hours
- 3OtroThe solvent was evaporated
- 4workup.ADDITIONthe residue was added to ice water, which
- 5Extracciónwas extracted with chloroform
- 6Lavadowashed with water
- 7Otrodried
- 8Otroevaporated
- 9OtroThe residue was purified by column chromatography on silica gel
Procedimiento
4-Chloro-3-methoxy-2-methylpyridine (3.14 g) was added to a solution of sodium (2.0 g) in ethanol (30 ml), and the solution was refluxed by heating for 10 hours. The solvent was evaporated and the residue was added to ice water, which was extracted with chloroform, washed with water, dried and evaporated. The residue was purified by column chromatography on silica gel, to give 4-ethoxy-3-methoxy-2-methyl-pyridine (2.6 g) as a light brown oil.