反応式
[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[CH:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]>CCOC(C)=O.[Pd]>[CH2:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:1][CH:2]1[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]参加物
4
実験手順
To a solution of ethyl 1,3-dihydro-2H-inden-2-ylideneacetate (302 mg, 1.49 mmol) in EtOAc (10 mL) was added 5% Pd/C (76 mg) and H2 was bubbled through the slurry for 20 h. The slurry was then filtered through Celite and the organic solution was concentrated in vacuo. Ethyl 2,3-dihydo-1H-inden-2-ylacetate (285 mg, 94%) was isolated as a colorless oil without purification.
後処理
- customwas bubbled through the slurry for 20 h
- filtrationThe slurry was then filtered through Celite
- concentrationthe organic solution was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-8c432927ddfc44d48430fe5fb7ac8288
- 出典データセット
- uspto-grants-2007_06
- 特許番号
- USRE039679E1
関連ノート
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