Reacción #660211

ord-dc0a9c05ed624003a7bdaffa1a49d96c

Disolventes

Condiciones de reacción

Temperatura
85°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was cooled to room temperature
  2. 2
    Otroin a water bath to quench
  3. 3
    Otrothe reaction
  4. 4
    ExtracciónThe mixture was extracted with chloroform (100 ml)
  5. 5
    Lavadowashed 3 times with 1N hydrochloric acid (30 ml), 3 times with 5% aqueous sodium hydrogen carbonate solution (30 ml)
  6. 6
    SecadoThe organic layer was dried over sodium sulfate
  7. 7
    Otrothe solvent of the filtrate was evaporated
  8. 8
    OtroThe residue was isolated
  9. 9
    Otropurified by silica gel column chromatography
  10. 10
    Otroprecipitated with methanol (70 ml)

Procedimiento

Sodium hydride (60%, 0.98 g, 24.5 mmol) washed with hexane was suspended in toluene (16 ml), 1-docosanol (4.00 g, 12.2 mmol) was added, 1,12-dibromododecane (8.04 g, 24.5 mmol) was added, and the mixture was stirred at 85° C. for 2 days. The reaction mixture was cooled to room temperature, 1N hydrochloric acid (30 ml) was added dropwise thereto in a water bath to quench the reaction. The mixture was extracted with chloroform (100 ml), and washed 3 times with 1N hydrochloric acid (30 ml), 3 times with 5% aqueous sodium hydrogen carbonate solution (30 ml), and once with 20% aqueous sodium chloride solution (30 ml). The organic layer was dried over sodium sulfate, and the solvent of the filtrate was evaporated. The residue was isolated and purified by silica gel column chromatography and precipitated with methanol (70 ml) to give 12-docosyloxy-dodecyl bromide (yield 78%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09029504B2uspto-grants-2015_05