(S)-2,4-diethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine → (S)-2,4-diethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-7-carboxylic acid
反応式
[CH2:1]([C@H:3]1[C:8](=[O:9])[N:7]([CH2:10][CH3:11])[C:6]2[CH:12]=[CH:13][C:14]([C:16]([O:18]C)=[O:17])=[CH:15][C:5]=2[O:4]1)[CH3:2]>Cl>[CH2:1]([C@H:3]1[C:8](=[O:9])[N:7]([CH2:10][CH3:11])[C:6]2[CH:12]=[CH:13][C:14]([C:16]([OH:18])=[O:17])=[CH:15][C:5]=2[O:4]1)[CH3:2]参加物
3
実験手順
A mixture of (S)-2,4-diethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (1.90 g) in concentrated hydrochloric acid (40 ml) was stirred under reflux for a day. The concentrated hydrochloric acid was distilled off under reduced pressure to give (S)-2,4-diethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-7-carboxylic acid (1.47 g).
後処理
- temperatureunder reflux for a day
- distillationThe concentrated hydrochloric acid was distilled off under reduced pressure
出典と根拠
- ORDレコード
- ord-dd073c96401043aeb09e1a4fdf2b4797
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05597820
反応ノート
読み込み中…