3-Methoxy-5-nitro-biphenyl → 5-Methoxy-[1,1'-biphenyl]-3-amine
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[C:7]([N+:9]([O-])=O)[CH:8]=1>C(O)C.[Pd]>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([NH2:9])[CH:6]=[C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:4]=1参加物
4
実験手順
3-Methoxy-5-nitro-biphenyl (176 mg, 0.77 mmol) are hydrogenated in ethanol (5 ml) using palladium on carbon (10%, 17 mg) at atmospheric pressure for 2 h. The calalyst is filtered off and the solvent removed in vacuo. Flash chromatography (silica, eluent ethyl acetate/cyclohexane 1:1) affords the product (139 mg, 91%) as a bown oil. MS: m/e=199 (M+).
後処理
- customfor 2 h
- filtrationThe calalyst is filtered off
- customthe solvent removed in vacuo
出典と根拠
- ORDレコード
- ord-99ed7f8006714ba4958423a72e34301f
- 出典データセット
- uspto-grants-2008_01
- 特許番号
- US07317007B2
反応ノート
読み込み中…