Реакция #64653

ord-2d79bf1e031f404cbd4495a86c976c85

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe mixture was filtered
  2. 2
    workup.ADDITIONthe filtrate was diluted with ethyl acetate
  3. 3
    Промывкаwashed with 3 times of water, brine
  4. 4
    СушкаThe solution was dried (Na2SO4)
  5. 5
    Другоеevaporated
  6. 6
    ДругоеThe residue was purified by flash chromotography on silica gel
  7. 7
    Промывкаeluting with 90:10 heptane

Методика

The title acid of Step 9 (5.2 g, 30 mmol) was dissolved in dimethylformamide (25 mL) and cooled to 0° C. To this solution potassium carbonate (5.7 g, 41.48 mmol) was added followed by benzyl bromide (5.7 g, 29.7 mmol). The mixture was stirred at room temperature overnight. The mixture was filtered and the filtrate was diluted with ethyl acetate, washed with 3 times of water, brine. The solution was dried (Na2SO4) and evaporated. The residue was purified by flash chromotography on silica gel, eluting with 90:10 heptane:ethyl acetate to give the pure title compound as colorless oil (4.5 g, 60% yield). 1H NMR: 300 MHz spectrum consistent with proposed structure. Anal: calcd. for C17H16O2 : C, 80.93; H, 6.39. Found: C, 80.69; H, 6.47.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05414018uspto-grants-1995_05