반응 #2025284

ord-b94f293045eb43a0b4a7586359dd7661

반응 방정식

O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
O=S([O-])O.[Na+]
sodium hydrogen sulfite
CC(=O)OC(C)Cc1ccc(-c2ccc(C(C)=O)cc2)cc1
(-)-4-acetyl-4'-(2-acetoxypropyl)biphenyl
ClC(Cl)Cl
CHCl3
O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
CC(=O)Oc1ccc(-c2ccc(CC(C)OC(C)=O)cc2)cc1
(-)-4-acetoxy-4'-(2-acetoxypropyl)biphenyl
수율 97.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타provided with a thermometer
  2. 2
    workup.DISSOLUTIONan agitator, and dissolved
  3. 3
    온도at reflux for 8 hours
  4. 4
    세척the organic layer was washed with 10% aqueous solution of sodium bicarbonate
  5. 5
    건조with water, and dried an anhydrous magnesium sulfate
  6. 6
    농축The resulting dichloromethane solution was concentrated under the reduced pressure

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05693251uspto-grants-1997_12