Nitric Acid → 4-Hydroxy-3-nitro-5,6,7,8-tetrahydroquinolin-2(1H)-one
反応式
[OH:1][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[NH:5][C:4](=[O:12])[CH:3]=1.[N+:13]([O-])([OH:15])=[O:14].O>C(O)(=O)C>[OH:1][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[NH:5][C:4](=[O:12])[C:3]=1[N+:13]([O-:15])=[O:14]参加物
5
実験手順
A solution of 4-hydroxy-5,6,7,8-tetrahydrocarbostyril (1.70g; 0.0103 mole) and concentrated nitric acid (2.5 ml; d 1.42), in glacial acetic acid (10 ml) was heated at 100° C till the oxides of nitrogen were evolved and rapidly cooled in ice. Water (40 ml) was added to the red solution to precipitate the yellow-orance 3-nitro derivative. After filtration, thorough washing with water and recrystallisation from acetic acid - ethanol the product had m.p. 241° (d).
後処理
- temperaturerapidly cooled in ice
- customto precipitate the yellow-orance 3-nitro derivative
- filtrationAfter filtration
- washthorough washing with water and recrystallisation from acetic acid - ethanol the product
出典と根拠
- ORDレコード
- ord-5684e01494ae42bbaba6a053dfeb86ec
- 出典データセット
- uspto-grants-1977_06
- 特許番号
- US04031099
反応ノート
読み込み中…