Nitric Acid → 6-Acetamido-3-butyl-5-nitro-phthalide
反応式
[N+:1]([O-:4])(O)=[O:2].[C:5]([NH:8][C:9]1[CH:18]=[C:17]2[C:12]([CH:13]([CH2:19][CH2:20][CH2:21][CH3:22])[O:14][C:15]2=[O:16])=[CH:11][CH:10]=1)(=[O:7])[CH3:6]>>[C:5]([NH:8][C:9]1[CH:18]=[C:17]2[C:12]([CH:13]([CH2:19][CH2:20][CH2:21][CH3:22])[O:14][C:15]2=[O:16])=[CH:11][C:10]=1[N+:1]([O-:4])=[O:2])(=[O:7])[CH3:6]参加物
3
実験手順
To 100 ml of stirred and ice-cold turning nitric acid (sp. gr. 1.50) there are added, in portions, 59 g (0.288 mol) of compound obtained in Example 7 with the temperature below 10° C. The resulting clear solution is put aside at room temperature overnight. The reaction material is poured into crushed ice, and the solid is filtered, washed with water, dried and crystallised from ethanol, giving the title compound.
後処理
- additionThe reaction material is poured
- custominto crushed ice
- filtrationthe solid is filtered
- washwashed with water
- customdried
- customcrystallised from ethanol
出典と根拠
- ORDレコード
- ord-aae83b5e83bf44a2b51f533fcb26b36a
- 出典データセット
- uspto-grants-2004_02
- 特許番号
- US06689808B2
反応ノート
読み込み中…