反応式
[CH:1]1([C:4]([C:6]2[CH:11]=[CH:10][C:9]([CH2:12][C:13]([OH:15])=[O:14])=[CH:8][CH:7]=2)=[O:5])[CH2:3][CH2:2]1.[CH3:16]O>S(=O)(=O)(O)O>[CH:1]1([C:4]([C:6]2[CH:11]=[CH:10][C:9]([CH2:12][C:13]([O:15][CH3:16])=[O:14])=[CH:8][CH:7]=2)=[O:5])[CH2:2][CH2:3]1参加物
4
実験手順
Dissolve 4-(cyclopropylcarbonyl)benzeneacetic acid in methanol (100 mL) containing concentrated sulfuric acid (10 drops). Stir 24 hours. Add triethylamine (2 mL) and concentrate the solution. Dissolve the residue in water/ethyl acetate. Wash the organic phase with saturated sodium hydrogen carbonate solution, dry over anhydrous magnesium sulfate and concentrate. Purify by silica gel chromatography (400 mL silica gel, 20% ethyl acetate/heptane as eluent) to give the title compound (4.6 g, 68%).
後処理
- concentrationAdd triethylamine (2 mL) and concentrate the solution
- dissolutionDissolve the residue in water/ethyl acetate
- washWash the organic phase with saturated sodium hydrogen carbonate solution
- dry with materialdry over anhydrous magnesium sulfate
- concentrationconcentrate
- customPurify by silica gel chromatography (400 mL silica gel, 20% ethyl acetate/heptane as eluent)
出典と根拠
- ORDレコード
- ord-ed34983475554c07bd2c082b862884c6
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06700012B2
関連ノート
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