Реакция #533580

ord-0e99c0e2e8f548b1a6fb9f6ef9c16959

Уравнение реакции

O=C([O-])[O-].[K+].[K+]
potassium carbonate
COC=Cc1cccc(Br)c1C
1-bromo-3-(2-methoxyvinyl)-2-methylbenzene
Cc1c(Br)cccc1CCO
subtitled compound
Cc1c(Br)cccc1CCO
2-(3-Bromo-2-methylphenyl)ethanol

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияthe solution was filtered
  2. 2
    workup.DISSOLUTIONdissolved/part
  3. 3
    workup.ADDITIONadded to the reaction mixture from above
  4. 4
    ДругоеA grey, cloudy, two-phase mixture was formed
  5. 5
    Экстракцияextracted twice with ethyl acetate
  6. 6
    ПромывкаThe combined organic phases were washed with brine
  7. 7
    Сушкаdried (MgSO4)
  8. 8
    Фильтрацияfiltered
  9. 9
    Концентрированиеconcentrated in vacuo

Методика

To an ice-cold solution of 1-bromo-3-(2-methoxyvinyl)-2-methylbenzene [Aromatic Intermediate 22, step a] (1.75 g) in THF (25 mL) was added a solution of mercury(II) acetate (2.95 g) in water (30 mL) and the resulting solution was stirred in ice-water for 2.75 hours. Meanwhile, potassium carbonate (35 g) was dissolved in water (30 mL) and the solution was filtered. Sodium borohydride (1.17 g) was part dissolved/part suspended in 35 mL of the resulting potassium carbonate solution, and added to the reaction mixture from above. A grey, cloudy, two-phase mixture was formed, that was stirred at room temperature for 2.5 hours, then poured into water and extracted twice with ethyl acetate. The combined organic phases were washed with brine, dried (MgSO4), filtered and concentrated in vacuo to afford the subtitled compound as a colourless oil. Yield 1.67 g.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08476265B2uspto-grants-2013_07