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Water → [3-Fluoro-4-(methylsulfanyl)phenyl]methanol

HRID 497268
ノート
印刷プレビュー

反応式

HRID 497268 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[S:10][CH3:11])[CH:5]=[O:6].[BH4-].[Na+].O>CO>[F:1][C:2]1[CH:3]=[C:4]([CH2:5][OH:6])[CH:7]=[CH:8][C:9]=1[S:10][CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 112752573-Fluoro-4-(methylthio)benzaldehyde

生成物 1

HCID 22316885[3-Fluoro-4-(methylsulfanyl)phenyl]methanol収率 101.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

The mixture of 3-fluoro-4-(methylsulfanyl)benzaldehyde (19.44 g, 114.2 mmol) and sodium borohydride (2.1 g, 55.46 mmol) in methanol (200 mL) was stirred at room temperature for 2 hour. Water was added to the mixture, and the mixture was evaporated, diluted with ethyl acetate (300 mL), washed with water (100 mL), dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate/hexane (1/4) to provide the subtitle compound (19.91 g, 100% yield) as an oil.

後処理

  1. customthe mixture was evaporated
  2. additiondiluted with ethyl acetate (300 mL)
  3. washwashed with water (100 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by flash chromatography on silica gel eluting with ethyl acetate/hexane (1/4)

出典と根拠

ORDレコード
ord-44c573b39f2141bd8761651864194c5e
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06949536B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート