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][C:16]([O:19]C)=[CH:15][CH:14]=2)=[O:12])=[O:10])=[CH:5][CH:4]=1>Br.CC([O-])=O>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([C:9](=[O:10])[C:11]([C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=2)=[O:12])=[CH:7][CH:8]=1参加物
4
実験手順
4,4′-dimethoxybenzil (2.0 g, 7.41 mmol) was dissolved in 30 mL of hydrogen bromide and 10 mL of acetic acid glacial. The reaction was stirred at reflux temperature overnight. The mixture was extracted with ethyl acetate and the organic phase was washed with water, dried over sodium sulphate. Concentration under vaccum gave the title compound as a yellow solid (1.9 g, quantitative).
後処理
- temperatureat reflux temperature overnight
- extractionThe mixture was extracted with ethyl acetate
- washthe organic phase was washed with water
- dry with materialdried over sodium sulphate
- concentrationConcentration under vaccum
出典と根拠
- ORDレコード
- ord-4a62e416177a4f4ebd82c7f82b8a06e7
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09353089B2
関連ノート
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