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

HRID 1742492ノート

反応式

HRID 1742492 の反応式
[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]

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-28b813f39a2d4eee824b832a8eb6fa1a
出典データセット
uspto-grants-1994_08
特許番号
US05338855

反応ノート

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