4-(Diethoxymethyl)benzaldehyde → 4-(Hydroxymethyl)benzaldehyde

HRID 230122

反応式

HRID 230122 の反応式
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

4

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

  1. customThe MeOH was removed
  2. additiondiluted with water
  3. extractionThe aqueous layer was extracted with DCM (3×50 mL)
  4. customThe combine organic layers were dried
  5. filtrationfiltered
  6. concentrationconcentrated
  7. dissolutionThe crude oil was dissolved in MeOH (50 mL)
  8. additionTo this was added 2N HCl (10.0 mL) in ether
  9. waitThe reaction mixture was left at room temperature for 24 hours
  10. customThe MeOH was removed
  11. customthe crude product was purified by flash column chromatography
  12. 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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