HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27681Erstellt: 24. Oktober 2026
Formamide → Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-
https://huagongshe.com/de/reaction/27681
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formamide | HCID 713 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Acetamide, N-[2-[2-(2-bromo-4,6-dinitrophenyl)diazenyl]-5-(diethylamino)phenyl]- | HCID 104287 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Katalysator | Cupric Chloride | HCID 24014 | — |
| Lösungsmittel | Butyl Acetate | HCID 31272 | — |
| Produkt | Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)- | HCID 90383 | 96% |
Reaktionsschritte
2-Bromo-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene (2.4 parts), copper (II) chloride (0.67 parts), anhydrous sodium acetate (1.2 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 for 5 hours after which time the reaction is complete. The mixture is cooled to room temperature and poured into petroleum-ether (boiling range 60-80°) (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 96% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04222935 |
|---|
| Quelldatensatz | uspto-grants-1980_09 |
|---|
| ORD ID | ord-a9221bcf0bbb4c9692966241d39232ec |
|---|
| Quellennotiz | uspto-grants-1980_09 |
|---|