Methyl iodide → HCID 20265013、化合物
反応式
[N+:1]([C:4]1[C:17]2[C:16](=[O:18])[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[NH:9][C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].[H-].[Na+].[CH3:21]I>CN(C)C=O>[CH3:21][N:9]1[C:10]2[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=2)[C:16](=[O:18])[C:17]2[C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=[CH:7][C:8]1=2参加物
5
実験手順
4.8 g of 1-nitro-9-acridanone are dissolved in 200 ml of dimethylformamide and treated with 0.5 g of sodium hydride. The deep red solution is treated with 2.5 ml of methyl iodide and stirred at room temperature for 4 hours. The yellow precipitate obtained is filtered and washed successively with dimethylformamide, water, ethanol and ether. There is obtained 10-methyl-1-nitro-9-acridanone of melting point 308°-309°.
後処理
- customThe yellow precipitate obtained
- filtrationis filtered
- washwashed successively with dimethylformamide, water, ethanol and ether
出典と根拠
- ORDレコード
- ord-f447da1f560c46aaa2e9b4783110f236
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04544659
反応ノート
読み込み中…