Реакция #55958
ord-93bd652589b648a7801ab04648adafb1
Уравнение реакции
2-Bromo-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino) azobenzene
potassium acetate
formamide
acetic anhydride
→
2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Выход 95.0%
Реактанты
Реагенты
Растворители
Условия реакции
Температура
110°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураheated
- 2ТемператураThe temperature is maintained at 110° C. for 2 hours
- 3Другоеwhen reaction
- 4ТемператураThe mixture is cooled to room temperature
- 5ДругоеThe precipitate is collected
- 6Промывкаwashed with petroleum ether (100 parts)
- 7Другоеdried
Методика
2-Bromo-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino) azobenzene (2.4 parts), copper (I) iodide (0.95 parts), anhydrous potassium acetate (1.5 parts), formamide (1.8 parts), acetic anhydride (2.0 parts) and n-butyl acetate (44 parts) are mixed together and heated, with stirring, to 110° C. during 15 minutes. The temperature is maintained at 110° C. for 2 hours when reaction is complete. The mixture is cooled to room temperature and poured into petroleum ether (boiling range 60-80° C.) (400 parts). The precipitate is collected, washed with petroleum ether (100 parts) and dried. 2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene is obtained in 95% yield.