Acetic Acid → 2-Methoxy-4-(methylamino)-5-nitrophenol
反応式
[CH3:1][NH:2][C:3]1[CH:8]=[C:7]2[O:9][CH2:10][O:11][C:6]2=[CH:5][C:4]=1[N+:12]([O-:14])=[O:13].C[O-].[Na+].C(O)(=O)C>CO.O>[CH3:10][O:9][C:7]1[CH:8]=[C:3]([NH:2][CH3:1])[C:4]([N+:12]([O-:14])=[O:13])=[CH:5][C:6]=1[OH:11]参加物
6
実験手順
A solution of 0.1 mol (19.6 g) of 2-methylamino-4,5-methylenedioxy-1-nitrobenzene, prepared according to Example 3, in 80 ml of a 30% strength solution of sodium methylate in methanol is brought for 15 minutes to the refluxing temperature of the methanol. The reaction medium is diluted with 500 ml of water. After the filtrate has been neutralized with acetic acid, the expected product precipitates.
後処理
- customthe expected product precipitates
出典と根拠
- ORDレコード
- ord-9264688154a34f7aa552f22b3eac3875
- 出典データセット
- uspto-grants-1988_06
- 特許番号
- US04749379
反応ノート
読み込み中…