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

HRID 1880328

反応式

HRID 1880328 の反応式
[C:1]1([NH:7][N:8]=[CH:9][C:10](=[O:12])[CH3:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:13]([CH:15]=O)=[O:14]>C(O)(=O)C>[OH:12][C:10]1[C:9]([C:13](=[O:14])[CH3:15])=[N:8][N:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH:11]=1

参加物

4

反応物 2

HCID 7860GlyoxalHCID 2204342-Oxopropanal phenylhydrazone

生成物 1

HCID 134133951-(4-hydroxy-1-phenyl-1H-pyrazol-3-yl)ethanone収率 43.4%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

To 2-oxopropanal phenylhydrazone (5.00 g, 30.8 mmol) in acetic acid (60 mL) was added a 40% aqueous solution of glyoxal (5.9 g, 4.6 mL, 30.8 mmol) and the mixture was heated at reflux for 45 minutes. The acetic acid was removed under reduced pressure. The resultant mixture was diluted with ethyl acetate (100 mL), washed with NaHCO3 and sat. aq. NaCl. Solids were removed by filtration, the filtrate was dried over Na2SO4, filtered and concentrated. The crude material was purified by CombiFlash (180 g column, 0-20 EtOAc/heptane gradient) to afford 1-(4-hydroxy-1-phenyl-1H-pyrazol-3-yl)ethanone as a yellow solid (2.70 g, 43%).

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 45 minutes
  3. customThe acetic acid was removed under reduced pressure
  4. additionThe resultant mixture was diluted with ethyl acetate (100 mL)
  5. washwashed with NaHCO3 and sat. aq. NaCl
  6. customSolids were removed by filtration
  7. dry with materialthe filtrate was dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude material was purified by CombiFlash (180 g column, 0-20 EtOAc/heptane gradient)

出典と根拠

ORDレコード
ord-4685bdcabab04375a1f86305a6097dba
出典データセット
uspto-grants-2012_11
特許番号
US08318762B2

関連ノート

読み込み中…