1-Methanesulfonyl-3-nitro-5-trifluoromethylbenzene → 3-Methanesulfonyl-5-(trifluoromethyl)aniline
反応式
[CH3:1][S:2]([C:5]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[C:7]([N+:15]([O-])=O)[CH:6]=1)(=[O:4])=[O:3]>CO.[Pd]>[CH3:1][S:2]([C:5]1[CH:6]=[C:7]([NH2:15])[CH:8]=[C:9]([C:11]([F:12])([F:14])[F:13])[CH:10]=1)(=[O:3])=[O:4]参加物
4
実験手順
1-methanesulfonyl-3-nitro-5-trifluoromethylbenzene (500 mg; 1.9 mmol) was dissolved in 100 mL methanol, 70 mg of Pd/C (10%) was added and the mixture was hydrogenated at 3 bar. The reaction mixture was filtrated and solvent removed under reduced pressure. 250 mg (1.04 mmol; 55% yield) of a colorless solid were obtained.
後処理
- filtrationThe reaction mixture was filtrated
- customsolvent removed under reduced pressure
- custom250 mg (1.04 mmol; 55% yield) of a colorless solid were obtained
出典と根拠
- ORDレコード
- ord-60e9a96934eb4903941ccf52a1d46f91
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08410100B2
反応ノート
読み込み中…