反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:11][CH3:12])=[C:6]([CH:9]=1)[CH2:7][OH:8].[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:11][CH3:12])=[C:6]([CH:9]=1)[CH:7]=[O:8]参加物
4
実験手順
5-Bromo-2-ethoxybenzyl alcohol (2.78 g, 12.0 mmol) and pyridinium dichromate (4.51 g, 12.0 mmol) in 120 ml of CH2Cl2 was stirred at RT for 6 h. The mixture was filtered, washed with H2O, 0.5N HCl and brine and dried over Na2SO4. The product was purified by silica gel column chromatography (EtOAc/petroleum ether 10:100) to give 5-bromo-2-ethoxybenzaldehyde.
後処理
- filtrationThe mixture was filtered
- washwashed with H2O, 0.5N HCl and brine
- dry with materialdried over Na2SO4
- customThe product was purified by silica gel column chromatography (EtOAc/petroleum ether 10:100)
出典と根拠
- ORDレコード
- ord-14ed117b41fe4638a869c64991c7f68e
- 出典データセット
- uspto-grants-1998_02
- 特許番号
- US05714503
関連ノート
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