HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1071781Erstellt: 27. Oktober 2026
Pyridine → N-{4[(acetyloxy)imino]-2,5-cyclohexadien-1-ylidene}aniline
https://huagongshe.com/reaction/1071781
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | 4-Nitrosodiphenylamine | HCID 9074 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-{4[(acetyloxy)imino]-2,5-cyclohexadien-1-ylidene}aniline | HCID 20801492 | — |
Reaktionsschritte
A solution was prepared by mixing 4-nitrosodiphenylamine, 19.8 grams, (0.10 mole), pyridine, 8.6 grams, (0.11 mole), and toluene, 10 mL, in a suitable reaction flask. The solution was cooled to 5° C. and acetic anhydride, 11.22 grams, (0.11 mole) was added slowly. The mixture was stirred for 2 hours and allowed to come to room temperature. The reaction mixture was mixed with a quantity of water, allowed to stand until the water layer separated, and the water layer was discarded. The toluene solution was evaporated to leave 21.4 grams of a solid residue, 96% of theory. The material melted at 63-65° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06906121B2 |
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| Quelldatensatz | uspto-grants-2005_06 |
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| ORD ID | ord-ec5e0582668946a39c1d9a9f080e78be |
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| Quellennotiz | uspto-grants-2005_06 |
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