反応式
[CH3:1][N:2]([CH3:13])[C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:12])[CH3:11])=[CH:5][CH:4]=1.[N+:14]([O-])([OH:16])=[O:15].OS(O)(=O)=O>>[CH3:13][N:2]([CH3:1])[C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=[O:12])[CH3:11])=[C:5]([N+:14]([O-:16])=[O:15])[CH:4]=1参加物
4
実験手順
N-[4-(dimethylamino)phenyl]acetamide obtained in step I above was nitrated using nitric acid (1.2 eq)+H2SO4 (1.0 eq) at 0 to 5° C. for 2 hrs. After the completion of the reaction, reaction mixture was added to ice and pH was adjusted to 8, extracted with dichloromethane, which was evaporated to dryness to obtain N-[4-(dimethylamino)-2-nitrophenyl]acetamide.
後処理
- customat 0 to 5° C.
- customfor 2 hrs
- customAfter the completion of the reaction, reaction mixture
- additionwas added to ice and pH
- extractionextracted with dichloromethane, which
- customwas evaporated to dryness
出典と根拠
- ORDレコード
- ord-d2a14774e774469797592a2ed1dfd384
- 出典データセット
- uspto-grants-2013_05
- 特許番号
- US08440830B2
関連ノート
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