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Water → (4-Fluorophenyl)(2-thienyl)methanol

HRID 439831
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인쇄 미리보기

반응식

HRID 439831 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[F:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]([C:16]2[S:17][CH:18]=[CH:19][CH:20]=2)=[O:15])=[CH:10][CH:9]=1.O.[OH-].[Na+]>C1COCC1>[F:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]([C:16]2[S:17][CH:18]=[CH:19][CH:20]=2)[OH:15])=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 684794-Fluorophenyl 2-thienyl ketoneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 10987480(4-Fluorophenyl)(2-thienyl)methanol수율 99%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

Lithium aluminium hydride (3.68 g, 97 mmol) was added portionwise to a stirred solution of (4-fluorophenyl)-(2-thienyl)ketone (10.0 g, 48.5 mmol) in dry THF (160 ml) at room temperature under argon. The mixture was stirred overnight and water (3.7 ml) added dropwise with caution. After 0.5 h 15% aqueous sodium hydroxide (3.7 ml) was added and the mixture stirred for 0.5 h, finally water (11 ml) was added and the mixture stirred for 0.5 h. The precipitate was removed by filtration through celite and the flitrate was concentrated under reduced pressure to give (4-fluorophenyl)-(2-thienyl)methanol (10.0 g, 99%) as a yellow oil.

후처리

  1. stirringthe mixture stirred for 0.5 h
  2. stirringthe mixture stirred for 0.5 h
  3. customThe precipitate was removed by filtration through celite
  4. concentrationthe flitrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-f1789b4911b546f191c323347b3f4f65
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05516783

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