反応式
[Br:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[C:5](N)=[C:4]([I:12])[CH:3]=1.S(=O)(=O)(O)O.N([O-])=O.[Na+]>C(O)C.S([O-])([O-])(=O)=O.[Cu+2]>[Br:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:5]=[C:4]([I:12])[CH:3]=1参加物
実験手順
4-bromo-2-iodo-6-nitroaniline (5 g, 0.0145 mol) was added in portions to stirred concentrated sulfuric acid (60 ml) keeping the temperature at 0-5° C. After stirring in the cold for 1 h, sodium nitrite (2.3 g, 0.0326 mol) was added and the reaction mixture stirred in the cold for a further 2 h. The reaction mixture was then poured into ice (250 ml). The resultant mixture was added, in portions, to a boiling solution of copper (II) sulfate (0.36 g, 0.00145 mol) in ethanol (150 ml) and boiled for a further 2 h. The reaction mixture was cooled to ambient temperature and extracted with ethyl acetate (300 ml) which was washed with saturated sodium hydrogen carbonate solution (250 ml) and dried (MgSO4). The solvent was removed in vacuo to give 3-Bromo-5-iodonitrobenzene as a yellow solid (4.21 g, 88%) which was used without further purification.
後処理
- customat 0-5° C
- stirringthe reaction mixture stirred in the cold for a further 2 h
- waitboiled for a further 2 h
- extractionextracted with ethyl acetate (300 ml) which
- washwas washed with saturated sodium hydrogen carbonate solution (250 ml)
- dry with materialdried (MgSO4)
- customThe solvent was removed in vacuo
出典と根拠
- ORDレコード
- ord-fbdcd0b6528b4e158f922d5e93210d8c
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08481544B2
関連ノート
読み込み中…