Реакция #40886

ord-6954c721ef9f486e9691b22e474bc1ae

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGto stir for a further 24 h
  2. 2
    Промывкаwashed with water
  3. 3
    ЭкстракцияThe aqueous fraction was re-extracted three times with ethyl acetate
  4. 4
    Промывкаthe combined organic fractions washed three times with water
  5. 5
    Сушкаdried over sodium sulfate
  6. 6
    Фильтрацияfiltered
  7. 7
    Концентрированиеconcentrated in vacuo

Методика

Intermediate 2 (667 mg, 2.81 mmol) was dissolved in dimethylformamide (14 ml), 2-bromo-1-phenylethanone (560 mg, 2.81 mmol) was added and the reaction stirred for 24 h at room temperature. Water (5 ml) was added and the reaction allowed to stir for a further 24 h. The mixture was then diluted with ethyl acetate (100 ml) and washed with water. The aqueous fraction was re-extracted three times with ethyl acetate and the combined organic fractions washed three times with water, then dried over sodium sulfate, filtered and concentrated in vacuo. Column chromatography (10-20% ethyl acetate/hexanes) provided the title compound as a pale yellow oil (428 mg, 50%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07728022B2uspto-grants-2010_06