反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[CH:8][CH:7]=[CH:6]2.[OH:13]O>C(O)(=O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N+:9]([O-:13])=[CH:8][CH:7]=[CH:6]2参加物
4
反応条件
- 温度
- 100 °C
実験手順
6-Methoxy quinoline (15 g, 0.094 mol) was dissolved in acetic acid (97 ml) and treated with hydrogen peroxide (37 ml). The mixture was stirred to 100° C. for 2 hours. After evaporation to dryness 100 ml of water was added to the residue until a precipitate appears. Filtration and washing with water gives a yellow precipitate that is dried under vacuum to yield 13.5 g of the title compound as a light yellow solid (82%). MS (m/e): 176.3 (M+H)+.
後処理
- customAfter evaporation to dryness 100 ml of water
- additionwas added to the residue until a precipitate
- filtrationFiltration
- washwashing with water
- customgives a yellow precipitate that
- customis dried under vacuum
出典と根拠
- ORDレコード
- ord-7d4c626e781c45508d7b39a81a93de5c
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07534891B2
関連ノート
読み込み中…