反応式
[CH2:1]([O:3][C:4]1[C:5]([CH3:10])=[N:6][CH:7]=[CH:8][CH:9]=1)[CH3:2].[N+:11]([O-])([OH:13])=[O:12]>S(=O)(=O)(O)O>[CH2:1]([O:3][C:4]1[C:5]([CH3:10])=[N:6][C:7]([N+:11]([O-:13])=[O:12])=[CH:8][CH:9]=1)[CH3:2]参加物
4
実験手順
3-Ethoxy-2-methylpyridine (132.5 g) was added dropwise to concentrated sulphuric acid (530 ml) with stirring and cooling to keep the mixture below 10° C. A mixture of concentrated nitric acid (81 ml) and concentrated sulphuric acid (97 ml) was added dropwise over 4 hours, keeping the temperature below 5° C. The reaction mixture was allowed to warm up slowly to ambient temperature and then added in portions to ice/water (2.5 l). The solid was collected by filtration, washed with water and dried under vacuum at 50° C. to give 3-ethoxy-2-methyl-6-nitropyridine, m.p. 82°-84° C.
後処理
- temperaturecooling
- customthe mixture below 10° C
- additionwas added dropwise over 4 hours
- customthe temperature below 5° C
- filtrationThe solid was collected by filtration
- washwashed with water
- customdried under vacuum at 50° C.
出典と根拠
- ORDレコード
- ord-c3a8131bb97e458d8ebfefbe5a1eecc9
- 出典データセット
- uspto-grants-1995_11
- 特許番号
- US05464781
関連ノート
読み込み中…