1-(4-Methoxy-phenyl)-2-phenyl-ethane-1,2-dione → 1-(4-Hydroxyphenyl)-2-phenylethane-1,2-dione

HRID 436386노트

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HRID 436386 반응식
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([C:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[O:12])=[O:10])=[CH:5][CH:4]=1>C(O)(=O)C.Br>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]([C:11]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)=[O:12])=[O:10])=[CH:7][CH:8]=1

참가 물질

4

실험 절차

A solution of 50 g (0.21 mole) of 4-methoxybenzil in 250 ml of acetic acid and 300 ml of 48% hydrobromic acid was heated to reflux for 10 hours. A solid that separated on cooling was recovered by filtration and the filtrate extracted with ether. The solid was dissolved in ether, the ether solutions combined and extracted with 10 % potassium hydroxide. The potassium hydroxide solution was washed with ether and neutralized with hydrochloric acid. The resulting solid was dissolved in ether, the solution dried over magnesium sulfate, and the ether removed by distillation. The resulting dark, brown solid was recrystallized from benzene to yield 30 g (64%) of 4-hydroxybenzil; mp, 138°-140°, lit., 129°-130°.

후처리

  1. temperatureto reflux for 10 hours
  2. customA solid that separated
  3. temperatureon cooling
  4. filtrationwas recovered by filtration
  5. extractionthe filtrate extracted with ether
  6. dissolutionThe solid was dissolved in ether
  7. extractionextracted with 10 % potassium hydroxide
  8. washThe potassium hydroxide solution was washed with ether and neutralized with hydrochloric acid
  9. dissolutionThe resulting solid was dissolved in ether
  10. dry with materialthe solution dried over magnesium sulfate
  11. customthe ether removed by distillation
  12. customThe resulting dark, brown solid was recrystallized from benzene

출처 및 근거

ORD 기록
ord-1ee3d897b8344d54a925ab5f54df1920
출처 데이터셋
uspto-grants-1977_02
특허 번호
US04009040

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