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Tetrabutylammonium Fluoride → 4-(4-Chloro-phenyl)-4-methoxy-butan-1-ol

HRID 1643308
ノート
印刷プレビュー

反応式

HRID 1643308 の反応式
C([Si]([O:18][CH2:19][CH2:20][CH2:21][CH:22]([C:25]1[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][CH:26]=1)[O:23][CH3:24])(C1C=CC=CC=1)C1C=CC=CC=1)(C)(C)C.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[Cl:31][C:28]1[CH:27]=[CH:26][C:25]([CH:22]([O:23][CH3:24])[CH2:21][CH2:20][CH2:19][OH:18])=[CH:30][CH:29]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 2724141Tetrabutylammonium FluorideHCID 59568823tert-Butyl-[4-(4-chloro-phenyl)-4-methoxy-butoxy]-diphenyl-silane

生成物 1

HCID 595687954-(4-Chloro-phenyl)-4-methoxy-butan-1-ol収率 74.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of tert-butyl-[4-(4-chloro-phenyl)-4-methoxy-butoxy]-diphenyl-silane (343 mg, 0.75 mmol) in 20 mL THF was added at room temperature TBAF (7.5 mL, 7.5 mmol, 1M in THF). The mixture was stirred for 3 h and the reaction quenched by the addition of 10 mL saturated aqueous NH4Cl. The mixture was extracted with ethyl acetate (3×15 mL) and the combined organic layers washed with brine (2×10 mL) and dried over Na2SO4. The mixture was concentrated and the product isolated by flash column chromatography eluting with 6% to 60% ethyl acetate/hexane to provide 120 mg of the title compound.

後処理

  1. customthe reaction quenched by the addition of 10 mL saturated aqueous NH4Cl
  2. extractionThe mixture was extracted with ethyl acetate (3×15 mL)
  3. washthe combined organic layers washed with brine (2×10 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationThe mixture was concentrated
  6. customthe product isolated by flash column chromatography
  7. washeluting with 6% to 60% ethyl acetate/hexane

出典と根拠

ORDレコード
ord-06d9f148be9243c3907ec2bbbc8fdd9f
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08119692B2

反応ノート

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