1-(4-Methoxy-phenyl)-2-phenyl-ethane-1,2-dione → 1-(4-Hydroxyphenyl)-2-phenylethane-1,2-dione
反応式
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]=1参加物
4
実験手順
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°.
後処理
- temperatureto reflux for 10 hours
- customA solid that separated
- temperatureon cooling
- filtrationwas recovered by filtration
- extractionthe filtrate extracted with ether
- dissolutionThe solid was dissolved in ether
- extractionextracted with 10 % potassium hydroxide
- washThe potassium hydroxide solution was washed with ether and neutralized with hydrochloric acid
- dissolutionThe resulting solid was dissolved in ether
- dry with materialthe solution dried over magnesium sulfate
- customthe ether removed by distillation
- customThe resulting dark, brown solid was recrystallized from benzene
出典と根拠
- ORDレコード
- ord-1ee3d897b8344d54a925ab5f54df1920
- 出典データセット
- uspto-grants-1977_02
- 特許番号
- US04009040
反応ノート
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