2-[4-(2-Ethoxycarbonylvinyl)naphthyl]dioxolane → 2-[4-(2-Ethoxycarbonylethyl)naphthyl]dioxolane
反応式
[CH2:1]([O:3][C:4]([CH:6]=[CH:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11]([CH:18]2[O:22][CH2:21][CH2:20][O:19]2)=[CH:10][CH:9]=1)=[O:5])[CH3:2]>C(OCC)(=O)C.[Pd]>[CH2:1]([O:3][C:4]([CH2:6][CH2:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11]([CH:18]2[O:19][CH2:20][CH2:21][O:22]2)=[CH:10][CH:9]=1)=[O:5])[CH3:2]参加物
4
実験手順
To a solution of 2-[4-(2-ethoxycarbonylvinyl)naphthyl]dioxolane (701 mg, 2.35 mmol) in ethyl acetate (15 mL) was added palladium (5% on BaCO3, 51 mg). The mixture was stirred under a hydrogen atmosphere for 16 hr, filtered by suction through Celite and concentrated to provide 689 mg (98%) of a colorless oil.
後処理
- filtrationfiltered by suction through Celite
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-7f176542c60f46da9c62d93a4287629c
- 出典データセット
- uspto-grants-2003_09
- 特許番号
- US06613942B1
反応ノート
読み込み中…