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Glyoxal → 1-(1-benzyl-4-hydroxy-1H-pyrazol-3-yl)ethanone

HRID 1880338
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HRID 1880338 반응식
[CH:1]([CH:3]=O)=[O:2].[CH2:5]([NH:12][N:13]=[CH:14][C:15](=[O:17])[CH3:16])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>O.CO>[CH2:5]([N:12]1[CH:16]=[C:15]([OH:17])[C:14]([C:1](=[O:2])[CH3:3])=[N:13]1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7860GlyoxalHCID 669205262-Oxopropanal benzylhydrazone

생성물 1

HCID 669204761-(1-benzyl-4-hydroxy-1H-pyrazol-3-yl)ethanone수율 33%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

To a 40% aqueous solution of glyoxal (8.28 g, 6.55 mL, 57.1 mmol) was added a slurry of 2-oxopropanal benzylhydrazone (10.1 g, 57.1 mmol) in water (250 mL) and methanol (25 mL). The resulting mixture was heated at reflux for 3 hours before cooling to room temperature. The mixture was extracted with EtOAc (2×100 mL) and the combined organic extracts were washed with water, saturated aqueous NaCl, dried over Na2SO4, filtered and concentrated. The crude material was purified by CombiFlash (120 g column, 0-100% EtOAc/heptane gradient) to provide 1-(1-benzyl-4-hydroxy-1H-pyrazol-3-yl)ethanone (4.07 g, 33%).

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureat reflux for 3 hours
  3. extractionThe mixture was extracted with EtOAc (2×100 mL)
  4. washthe combined organic extracts were washed with water, saturated aqueous NaCl
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude material was purified by CombiFlash (120 g column, 0-100% EtOAc/heptane gradient)

출처 및 근거

ORD 기록
ord-5912bc2e12994f89ab829ab5ab074a93
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318762B2

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