Nitric Acid → n-(3-Chloro-4-nitrophenyl)acetamide
反応式
[N+:1]([O-:4])(O)=[O:2].[C:5]([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([Cl:15])[CH:10]=1)(=[O:7])[CH3:6]>O>[C:5]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([N+:1]([O-:4])=[O:2])=[C:11]([Cl:15])[CH:10]=1)(=[O:7])[CH3:6]参加物
4
実験手順
To fuming nitric acid (120 mL) at -50° C. was added N-acetyl-3-chloroaniline (30 g) over a period of 45 minutes. The reaction was kept between -50° C. and -30° C. using a dry ice/acetone bath. The reaction mixture was stirred for an additional hour and then poured into 1500 mL of crushed ice and water. The precipitate was filtered and slurried with 1 liter of slightly alkaline water (ammonium hydroxide) twice. The precipitate was then dried and recrystallized from toluene to yield (3.6 g) of N-acetyl-3-chloro-4-nitroaniline; m.p. 134°-136° C.
後処理
- customwas kept between -50° C. and -30° C.
- filtrationThe precipitate was filtered
- customThe precipitate was then dried
- customrecrystallized from toluene
出典と根拠
- ORDレコード
- ord-78a991295e1e4baf93b5315f3fafa37a
- 出典データセット
- uspto-grants-1991_07
- 特許番号
- US05034410
反応ノート
読み込み中…