反応式
[C:1]([CH:9]1[CH2:13][O:12][C:11](=[O:14])[CH2:10]1)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>CO.[Pd](Cl)Cl>[CH2:1]([CH:9]1[CH2:13][O:12][C:11](=[O:14])[CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
実験手順
To a solution of 4-benzoyl-dihydro-furan-2-one (5 g) in methanol (250 mL) in a Parr® reactor is added palladium chloride (0.25 g). The mixture is shaken under hydrogen (50 PSI) for 3 h. The mixture is filtered through a pad of Celite® (40 g) and the filtrate concentrated. The residue is chromatographed on SiO2 (10% ethyl acetate/hexanes, then 30% ethyl acetate/hexanes) to yield the title compound, (2.5 g, 34% from 3-benzoylpropionic acid), as a colorless liquid.
後処理
- filtrationThe mixture is filtered through a pad of Celite® (40 g)
- concentrationthe filtrate concentrated
- customThe residue is chromatographed on SiO2 (10% ethyl acetate/hexanes
出典と根拠
- ORDレコード
- ord-8b00c056f9bc46b2b56d079b375aa7cc
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087626B2
関連ノート
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