反応 #562983

ord-21029c2a780c4d12842cf4b74e4bf334

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas added dropwise
  2. 2
    その他The reaction mixture was quenched by the addition of a solution of ammonium chloride
  3. 3
    workup.ADDITIONEther was added
  4. 4
    その他the organic layer was collected
  5. 5
    乾燥dried (Na2SO4)
  6. 6
    濃縮concentrated
  7. 7
    その他The crude product was purified by column chromatography on silica gel

実験手順

A flask was charged with (3,5-difluorophenyl)magnesium bromide (149 mL, 149 mmol) and copper (I) iodide (1.901 g, 9.98 mmol). To this reaction mixture, 6-oxabicyclo[3.1.0]hexane (12.53 g, 149 mmol) dissolved in THF (25 mL) was added dropwise. The reaction mixture warmed upon the addition of the epoxide. The reaction was stirred at rt for 2 h at rt. The reaction mixture was quenched by the addition of a solution of ammonium chloride. Ether was added and the organic layer was collected, dried (Na2SO4) and concentrated. The crude product was purified by column chromatography on silica gel to afford (1S,2R)-2-(3,5-difluorophenyl)cyclopentanol (26.5 g, 134 mmol, 90% yield).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08637525B2uspto-grants-2014_01