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

HRID 1880338
ノート
印刷プレビュー

反応式

HRID 1880338 の反応式
[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
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 2

HCID 7860GlyoxalHCID 669205262-Oxopropanal benzylhydrazone

生成物 1

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

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

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%).

後処理

  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)

出典と根拠

ORDレコード
ord-5912bc2e12994f89ab829ab5ab074a93
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08318762B2

反応ノート

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