Реакция #2701

ord-bf0cea00f0c14b87bedbeafd627d9061

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with water (15 mL)
  2. 2
    СушкаThe organic layer was dried with MgSO4 and solvent
  3. 3
    Другоеwas removed under reduced pressure
  4. 4
    ДругоеThe crude material was purified by silicagel chromatography

Методика

To a cold (-78° C.), stirred solution of 1-(tol-4-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene (Compound B 1 g, 3.2 mmol), in THF (17 mL) was added t-BuLi in pentane (1.7M solution, 3 mL, 5.1 mmol). After 10 minutes dry dimethylformamide (DMF) (600 mg, 8 mmol) was added and the dry-ice cooling was replaced with ice-water bath. The mixture was gradually warmed to ambient temperature and diluted with ethylacetate (150 mL), washed with water (15 mL). The organic layer was dried with MgSO4 and solvent was removed under reduced pressure. The crude material was purified by silicagel chromatography to afford the title compound as a white solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05728846uspto-grants-1998_03