反応 #1739

ord-429d4cda5f5a43799ceb5fbb3c399100

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONthe reaction mixture was poured on to ice/saturated ammonium chloride solution
  2. 2
    抽出extracted with ethyl acetate
  3. 3
    その他The dark oil obtained
  4. 4
    その他after drying
  5. 5
    その他evaporation
  6. 6
    その他was purified by chromatography (RP18-LiChroprep, acetonitrile) and recrystallization from ethyl acetate

実験手順

100 mg of this ester were dissolved in 5 ml of absolute tetrahydrofuran and treated under argon with 104 mg of tetrakis-(triphenylphosphine)-palladium and 61 mg of tributyltin hydride. After stirring at room temperature for 30 min., the reaction mixture was poured on to ice/saturated ammonium chloride solution, acidified with 1N hydrochloric acid and extracted with ethyl acetate. The dark oil obtained after drying and evaporation was purified by chromatography (RP18-LiChroprep, acetonitrile) and recrystallization from ethyl acetate. There were obtained 21 mg of 6-[3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyloxy]-nicotinic acid in colorless crystals, m.p. 188°-190° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726191uspto-grants-1998_03