2-Hydroxy-5-nitroindane → 5-amino-2,3-dihydro-1H-inden-2-ol
反応式
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([OH:13])[CH2:7]2)([O-])=O>[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([OH:13])[CH2:7]2参加物
3
実験手順
5-nitro-indan-2-ol (450 mg, 2.5 mmol) was hydrogenated using Pd/C (10%, dry, 100 mg) and H2 balloon at 1 atm at room temperature. Pd/C was filtered off through a pad of celite and the mother liquid was concentrated to give the crude product, 5-Amino-indan-2-ol.
後処理
- customat room temperature
- filtrationPd/C was filtered off through a pad of celite
- concentrationthe mother liquid was concentrated
出典と根拠
- ORDレコード
- ord-c1e9be6881714f089dafe369bae5c784
- 出典データセット
- uspto-grants-2012_11
- 特許番号
- US08318790B2
反応ノート
読み込み中…