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Ethanol → (3-ethyl-1-methyl-1H-pyrazol-5-yl)methanol

HRID 530823
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인쇄 미리보기

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HRID 530823 반응식
[CH2:1]([C:3]1[CH:7]=[C:6]([C:8](OCC)=[O:9])[N:5]([CH3:13])[N:4]=1)[CH3:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].C(O)C.[Cl-].[NH4+]>C1COCC1>[CH2:1]([C:3]1[CH:7]=[C:6]([CH2:8][OH:9])[N:5]([CH3:13])[N:4]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 15131401Ethyl 3-ethyl-1-methyl-1H-pyrazole-5-carboxylateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 23005574(3-ethyl-1-methyl-1H-pyrazol-5-yl)methanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of compound 3 (2 g, 0.01 mol) in THF (20 mL) was added lithium aluminum hydride (0.63 g, 0.02 mol) at 0° C. and the mixture was stirred at room temperature for 30 min. Ethanol (10 mL) and saturated aqueous ammonium chloride solution (2.0 mL) were added to the reaction mixture. The precipitated insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel chromatography (ethyl acetate:hexane=1:1) to give the title compound as a colorless oil.

후처리

  1. filtrationThe precipitated insoluble material was filtered off
  2. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-22a6b5b04f6b4770965b41f0026b769a
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353104B2

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