Hydrochloric Acid → 4-Methoxy-3-(trifluoromethoxy)aniline
反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[C:6]([O:12][C:13]([F:16])([F:15])[F:14])[CH:5]=1)([O-])=O.Cl>CO.[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[C:6]([O:12][C:13]([F:14])([F:15])[F:16])[CH:5]=1参加物
5
実験手順
To a stirred solution of 4-nitro-2-trifluoromethoxyanisole (500 mg, 2.11 mmol) in MeOH (8.0 mL) at room temperature was added aqueous HCl solution (1.0 mL, 3.0 M) followed by 10% Pd/C (80 mg). The reaction mixture was stirred under H2 atmosphere for 17 h, filtered through a pad of celite and concentrated to give 4-amino-2-trifluoromethoxyanisole as a hydrochloride salt (500 mg). The product was used without further purification.
後処理
- filtrationfiltered through a pad of celite
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-2f4270a8cb01410c8810f851f3004318
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07691843B2
反応ノート
読み込み中…