Reacción #81495
ord-e264f97dc01f4627802db2c89be88394
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturato warm to room temperature
- 2workup.STIRRINGwith stirring
- 3Extracciónextracted with ether
- 4Lavadothe organic layer was washed with water (2x) and brine
- 5Secadodried over sodium sulfate
- 6ConcentraciónThe organic solution was concentrated
- 7Otrothe residue was purified by flash chromatography (chloroform/ethanol, 10:1)
Procedimiento
To a solution of 2-fluoro-6-methylpyridine (27 mmol) in 65 ml of freshly distilled THF was added via syringe 13.5 ml of 2M LDA, and the resulting mixture was stirred at -78° C. for 20 min. To the above cold solution was added 4 ml of 4M ethylene oxide and the mixture was allowed to warm to room temperature with stirring. The mixture was diluted with water, extracted with ether, and the organic layer was washed with water (2x) and brine, and dried over sodium sulfate. The organic solution was concentrated, and the residue was purified by flash chromatography (chloroform/ethanol, 10:1) to yield 1.3 g (30.9%) of 2-fluoro-6-(3-hydroxypropyl)pyridine, as a yellow oil.