反応 #2025284

ord-b94f293045eb43a0b4a7586359dd7661

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他provided with a thermometer
  2. 2
    workup.DISSOLUTIONan agitator, and dissolved
  3. 3
    温度at reflux for 8 hours
  4. 4
    洗浄the organic layer was washed with 10% aqueous solution of sodium bicarbonate
  5. 5
    乾燥with water, and dried an anhydrous magnesium sulfate
  6. 6
    濃縮The resulting dichloromethane solution was concentrated under the reduced pressure

実験手順

29.6 g (0.1 mol) of (-)-4-acetyl-4'-(2-acetoxypropyl)biphenyl (XIX-13) ([α]D20 =-9.9° (C=1, CHCl3)} was charged into a four necked-flask provided with a thermometer and an agitator, and dissolved by adding 200 ml of dichloromethane. 20.7 g (0.12 mol) of m-chloroperbenzoic acid was added in this solution and agitated at reflux for 8 hours. After excess of m-chloroperbenzoic acid was decomposed by adding 10% aqueous solution of sodium hydrogen sulfite to the reaction mixture, the organic layer was washed with 10% aqueous solution of sodium bicarbonate and then with water, and dried an anhydrous magnesium sulfate. The resulting dichloromethane solution was concentrated under the reduced pressure to provide 30.2 g (yield: 97%) of (-)-4-acetoxy-4'-(2-acetoxypropyl)biphenyl (XVIII-13).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05693251uspto-grants-1997_12