反応式
[F:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[N+:12]([O-])([OH:14])=[O:13]>S(=O)(=O)(O)O>[F:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([N+:12]([O-:14])=[O:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]参加物
4
実験手順
2,4-Difluorobenzoic acid (5 g, 0.031M) was dissolved in concentrated sulfuric acid (30 ml), and cooled to 0°. The mixture was stirred, and fuming nitric acid (d 1.567 g/ml, 1.91 ml, 0.047M) added dropwise, keeping the temperature below 5°. After stirring for 3 hours, the mix was poured onto ice, and organics extracted into dichloromethane (2×75 ml). The combined organic layers were washed with water, dried (MgSO4), and evaporated to give 2,4-difluoro-5-nitrobenzoic acid (3.9 g, 61%). Nmr (DHSO-d6): δ 7.18 (t, 1H); 8.88 (t, 1H); 9.93 (br, 1H).
後処理
- temperaturecooled to 0°
- customthe temperature below 5°
- stirringAfter stirring for 3 hours
- additionthe mix was poured onto ice
- extractionorganics extracted into dichloromethane (2×75 ml)
- washThe combined organic layers were washed with water
- dry with materialdried (MgSO4)
- customevaporated
出典と根拠
- ORDレコード
- ord-d37fd6ce2e1b46c8be875b8135b7ad5e
- 出典データセット
- uspto-grants-1997_07
- 特許番号
- US05652233
関連ノート
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