反応式
C([O:3][CH:4](OCC)[C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[O:10])=[CH:7][CH:6]=1)C.[BH4-].[Na+]>CO>[OH:10][CH2:9][C:8]1[CH:11]=[CH:12][C:5]([CH:4]=[O:3])=[CH:6][CH:7]=1参加物
反応条件
- 温度
- 0 °C
実験手順
To a cold (0° C.) solution of 4-(diethyoxymethyl)benzaldehyde (5.2 g, 24 mmol) in MeOH (50 mL) was added NaBH4 (0.93 g, 24 mmol), and the reaction mixture was stirred for 3 hours. The MeOH was removed and the residue was taken up in DCM and diluted with water. The aqueous layer was extracted with DCM (3×50 mL). The combine organic layers were dried, filtered and concentrated. The crude oil was dissolved in MeOH (50 mL) and cooled to 0° C. To this was added 2N HCl (10.0 mL) in ether. The reaction mixture was left at room temperature for 24 hours. The MeOH was removed and the crude product was purified by flash column chromatography, eluting with EtOAc/Hexane (3:7) to yield 2.92 g of 4-(hydroxymethyl)benzaldehyde (11) as a colorless oil.
後処理
- customThe MeOH was removed
- additiondiluted with water
- extractionThe aqueous layer was extracted with DCM (3×50 mL)
- customThe combine organic layers were dried
- filtrationfiltered
- concentrationconcentrated
- dissolutionThe crude oil was dissolved in MeOH (50 mL)
- additionTo this was added 2N HCl (10.0 mL) in ether
- waitThe reaction mixture was left at room temperature for 24 hours
- customThe MeOH was removed
- customthe crude product was purified by flash column chromatography
- washeluting with EtOAc/Hexane (3:7)
出典と根拠
- ORDレコード
- ord-ee732d22252346e6b92541f5244d0cef
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07566716B2
関連ノート
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