4-Nitroaniline → 2,3-Dibromo-N-[(4-nitrophenyl)carbamoyl]propanamide
反応式
[N+:1]([C:4]1[CH:10]=[CH:9][C:7]([NH2:8])=[CH:6][CH:5]=1)([O-:3])=[O:2].[Br:11][CH:12]([CH2:18][Br:19])[C:13]([N:15]=[C:16]=[O:17])=[O:14]>C(#N)C>[N+:1]([C:4]1[CH:10]=[CH:9][C:7]([NH:8][C:16]([NH:15][C:13](=[O:14])[CH:12]([Br:11])[CH2:18][Br:19])=[O:17])=[CH:6][CH:5]=1)([O-:3])=[O:2]参加物
4
反応条件
- 温度
- 20 °C
実験手順
14.0 g of 4-nitroaniline are dissolved in 200 ml of anhydrous acetonitrile, and 26.0 g of 2,3-dibromopropionyl isocyanate are added dropwise with cooling at 5° to 10° C. After stirring for 3 hours at 20° C., the solid precipitated is filtered off and dried. Yield: 35.0 g m.p.: 205° - 206° C. (decomp.).
後処理
- temperaturewith cooling at 5° to 10° C
- customthe solid precipitated
- filtrationis filtered off
- customdried
出典と根拠
- ORDレコード
- ord-748fbac827a44e89b2907f8c75a45eae
- 出典データセット
- uspto-grants-1977_07
- 特許番号
- US04036850
反応ノート
読み込み中…