Reacción #660211
ord-dc0a9c05ed624003a7bdaffa1a49d96c
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1TemperaturaThe reaction mixture was cooled to room temperature
- 2Otroin a water bath to quench
- 3Otrothe reaction
- 4ExtracciónThe mixture was extracted with chloroform (100 ml)
- 5Lavadowashed 3 times with 1N hydrochloric acid (30 ml), 3 times with 5% aqueous sodium hydrogen carbonate solution (30 ml)
- 6SecadoThe organic layer was dried over sodium sulfate
- 7Otrothe solvent of the filtrate was evaporated
- 8OtroThe residue was isolated
- 9Otropurified by silica gel column chromatography
- 10Otroprecipitated 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%).