反応式
[Br:1][C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH:3]=1.[N+:11]([O-:16])([N+]([O-])=O)=[O:12]>>[Br:1][C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[N+:11]([O-:16])=[O:12]参加物
3
実験手順
To a stirred 80 g. sample of solid 3-bromobenzofuran is added a large excess of dinitrogen tetraoxide. The mixture liquifies within 5 minutes. After 2 hours, the mixture is triturated with ethanol and filtered to provide yellow crystals of 3-bromo-2-nitrobenzofuran. The product is identical to the product of Example 1 according to infrared spectral analysis.
後処理
- waitAfter 2 hours
- customthe mixture is triturated with ethanol
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-b184488dbdaf49e1bc1525b04032eb7e
- 出典データセット
- uspto-grants-1979_03
- 特許番号
- US04144347
関連ノート
読み込み中…