反応式
O[N:2]=[C:3]1[CH2:8][CH2:7][CH:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:5][CH2:4]1.[ClH:15]>[Ni].C(O)C>[ClH:15].[C:9]1([CH:6]2[CH2:5][CH2:4][CH:3]([NH2:2])[CH2:8][CH2:7]2)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1参加物
5
実験手順
A mixture of 1-(hydroxyimino)-4-phenylcyclohexane (17.4 mmol) and Raney Nickel (300 mg) in ethanol was hydrogenated (90 psi) at 50° C. for 40 hours. The mixture was filtered through a pad of Celite, washed with MeOH, and concentrated. The residue was dissolved in MeOH, treated with HCl (4 N in dioxane, 20 mmol), and concentrated to give 4-phenylcyclohexylamine hydrochloride (100%).
後処理
- customat 50° C.
- customfor 40 hours
- filtrationThe mixture was filtered through a pad of Celite
- washwashed with MeOH
- concentrationconcentrated
- dissolutionThe residue was dissolved in MeOH
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-dce09784419a497ca6dc16664a00ebd5
- 出典データセット
- uspto-grants-2006_02
- 特許番号
- US06995269B2
関連ノート
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