HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1701273Erstellt: 26. Oktober 2026
Nitrone → Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-
https://huagongshe.com/reaction/1701273
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Nitrone | HCID 6350 | — |
| Edukt | Nitrobenzene | HCID 7416 | — |
| Edukt | 2,6-Lutidine | HCID 7937 | — |
| Edukt | Acetamide, N-[2-[2-(2-bromo-4,6-dinitrophenyl)diazenyl]-5-(diethylamino)phenyl]- | HCID 104287 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Produkt | Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)- | HCID 90383 | — |
Reaktionsschritte
A stirred mixture of 3-acetylamino-4-(2'-bromo-4',6'-dinitrophenylazo)-N,N-diethylaniline(4.8 parts), copper (I) iodide (2.0 parts), formaldoxime trimer (1.75 parts), 2,6-lutidine (2.15 parts), and nitrobenzene (150 parts) was heated to 95° C. for 10 hours when thin layer chromatography showed reaction to be complete. Isolation by the method of Example 1 gave 3-acetylamino-4-(2'-cyano-4',6'-dinitrophenylazo)-N,N-diethylaniline (infra red spectrum identical with that of authentic material). Similar results were obtained when the 2,6-lutidine was replaced by 2,4-lutidine (2.15 parts) and 2,4,6-collidine (2.4 parts).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04192800 |
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| Quelldatensatz | uspto-grants-1980_03 |
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| ORD ID | ord-4ddaf2075413441e9070d6e2574171fc |
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| Quellennotiz | uspto-grants-1980_03 |
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