Reacción #81495

ord-e264f97dc01f4627802db2c89be88394

Disolventes

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturato warm to room temperature
  2. 2
    workup.STIRRINGwith stirring
  3. 3
    Extracciónextracted with ether
  4. 4
    Lavadothe organic layer was washed with water (2x) and brine
  5. 5
    Secadodried over sodium sulfate
  6. 6
    ConcentraciónThe organic solution was concentrated
  7. 7
    Otrothe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05618821uspto-grants-1997_04