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Sodium Bicarbonate → (1-{1-[2,4-Bis(trifluoromethyl)phenyl]ethyl}piperidin-4-yl)methanol

HRID 1620554
ノート
印刷プレビュー

反応式

HRID 1620554 の反応式
[F:1][C:2]([F:24])([F:23])[C:3]1[CH:8]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:6]=[CH:5][C:4]=1[C:13]([N:15]1[CH2:20][CH2:19][CH:18]([CH2:21][OH:22])[CH2:17][CH2:16]1)=[CH2:14].[BH4-].[Na+].C(=O)([O-])O.[Na+]>CO>[F:23][C:2]([F:1])([F:24])[C:3]1[CH:8]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:6]=[CH:5][C:4]=1[CH:13]([N:15]1[CH2:16][CH2:17][CH:18]([CH2:21][OH:22])[CH2:19][CH2:20]1)[CH3:14]
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 516892Sodium BicarbonateHCID 4311764Sodium borohydrideHCID 86678734(1-{1-[2,4-Bis(trifluoromethyl)phenyl]ethenyl}piperidin-4-yl)methanol

生成物 1

HCID 86678735(1-{1-[2,4-Bis(trifluoromethyl)phenyl]ethyl}piperidin-4-yl)methanol収率 86%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of (1-{1-[2,4-bis(trifluoromethyl)phenyl]ethenyl}piperidin-4-yl)methanol (12.6 g) in methanol (178 mL) was added sodium borohydride (2.02 g). The reaction mixture was stirred at room temperature for 20 min, saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (10.9 g).

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-08494a3b9f0d4416bf3d8b0e1a6044c9
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08772277B2

反応ノート

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