Sodium Chloride → 2-(2,3,4,5-Tetramethoxy-6-methylphenyl)ethanol

HRID 1742492노트

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HRID 1742492 반응식
[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[C:7]([O:11][CH3:12])[C:6]([O:13][CH3:14])=[C:5]([CH3:15])[C:4]=1[CH2:16][CH:17]=[O:18].[BH4-].[Na+].[Cl-].[Na+]>C(O)C>[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[C:7]([O:11][CH3:12])[C:6]([O:13][CH3:14])=[C:5]([CH3:15])[C:4]=1[CH2:16][CH2:17][OH:18]

참가 물질

5

반응물 3

HCID 5234Sodium ChlorideHCID 4311764Sodium borohydrideHCID 190092572-(2,3,4,5-Tetramethoxy-6-methylphenyl)acetaldehyde

생성물 1

HCID 190092632-(2,3,4,5-Tetramethoxy-6-methylphenyl)ethanol수율 97.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

5.38 g of 2-(2,3,4,5-tetramethoxy-6-methylphenyl)acetaldehyde [prepared as described in step (b)-above] were dissolved in 60 ml of ethanol and reduced using 400 mg of sodium borohydride at 0° C. 150 ml of a saturated aqueous solution of sodium chloride were then added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated to dryness by evaporation under reduced pressure, to give a crude product. This crude product was then purified by column chromatography through silica gel, using a gradient elution method with mixtures of hexane and ethyl acetate ranging from 5:1 to 2:1 by volume as the eluent, to give 5.27 g of the title compound as a colorless oil.

후처리

  1. customat 0° C
  2. extractionthe mixture was extracted with ethyl acetate
  3. dry with materialThe extract was dried over anhydrous magnesium sulfate
  4. concentrationconcentrated to dryness by evaporation under reduced pressure
  5. customto give a crude product
  6. customThis crude product was then purified by column chromatography through silica gel
  7. washa gradient elution method with mixtures of hexane and ethyl acetate ranging from 5:1 to 2:1 by volume as the eluent

출처 및 근거

ORD 기록
ord-28b813f39a2d4eee824b832a8eb6fa1a
출처 데이터셋
uspto-grants-1994_08
특허 번호
US05338855

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