Реакция #162038

ord-678d897e5d754f00933640dabee675df

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe mixture was stirred overnight at room temperature
  2. 2
    Промывкаthe solution was washed with brine (50 mL)
  3. 3
    ЭкстракцияThe aqueous phase was extracted with toluene (30 mL) before all organic phases
  4. 4
    Сушкаdried (Na2SO4)
  5. 5
    Другоеthe solvent evaporated
  6. 6
    ДругоеThe crude product was purified

Методика

Cholestanol (0.662 g, 1.703 mmol) was dissolved in toluene (13 mL). Potassium tert-butoxide (573 mg, 5.11 mmol) was added in one portion. The mixture was stirred at room temperature for 3 hours. tert-Butyl bromoacetate (503 μL, 3.406 mmol) was added drop-wise and the mixture was stirred overnight at room temperature. Toluene (20 mL) was added and the solution was washed with brine (50 mL). The aqueous phase was extracted with toluene (30 mL) before all organic phases were combined, dried (Na2SO4) and the solvent evaporated. The crude product was purified using column chromatography (SiO2; Hexane:EtOAc, 200:1 to 200:20) to yield the white solid product (0.65 g, 76% yield). 1H NMR (400 MHz, CDCl3) δ: 3.98 (s, 2H, CH2O), 3.30 (m, 1H, CHO), 1.97-0.56 (m, 31H), 1.46 (s, 9H, CH3), 0.89 (d, 3H, J=6.1, CH3), 0.85 (d, 3H, J=2.0, CH3), 0.84 (d, 3H, J=1.4, CH3), 0.79 (s, 3H, CH3), 0.64 (s, 3H, CH3).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08828952B2uspto-grants-2014_09