1-Bromo-4-fluoro-5-methyl-2-nitrobenzene → 2-Bromo-5-fluoro-4-methylaniline
反応式
[Br:1][C:2]1[C:3]([N+:10]([O-])=O)=[CH:4][C:5]([F:9])=[C:6]([CH3:8])[CH:7]=1>C(O)(=O)C.[Fe]>[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([F:9])=[CH:4][C:3]=1[NH2:10]参加物
4
反応条件
- 温度
- 70 °C
実験手順
Iron powder (18.5 g) was added to a solution of 5-bromo-2-fluoro-4-nitrotoluene (9.7 g) in acetic acid (30 ml), and the mixture was stirred at 70° C. for 3 hours. The catalyst was removed by filtration through Celite, and the filtrate was washed with chloroform. The solvent and the like in the filtrate were distilled off under reduced pressure. The residue was subjected to column chromatography on silica gel to conduct elution with chloroform, thereby obtaining the title compound (7.9 g) as a red oil.
後処理
- customThe catalyst was removed by filtration through Celite
- washthe filtrate was washed with chloroform
- distillationThe solvent and the like in the filtrate were distilled off under reduced pressure
- washelution with chloroform
出典と根拠
- ORDレコード
- ord-b35a5741b64740b282bda99be200b36e
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06136823
反応ノート
読み込み中…