HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231127Erstellt: 24. Oktober 2026
Water → 4,5-Dihydro-4-oxo-N-phenyl-2-(phenylamino)-3-furancarboxamide
https://huagongshe.com/de/reaction/231127
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Phenyl isocyanate | HCID 7672 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-Bromo-3-oxo-n-phenylbutanamide | HCID 268268 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 4,5-Dihydro-4-oxo-N-phenyl-2-(phenylamino)-3-furancarboxamide | HCID 14198535 | — |
Reaktionsschritte
Under a nitrogen atmosphere, sodium hydride (97%; 0.633 g, 25.61 mmol) was weighed into a dry reaction vessel and covered with 55 ml of anhydrous dioxane. A solution of phenyl isocyanate (1.39 ml, 12.81 mmol) in 5 ml of anhydrous dioxane was then added over a 5-10 minute period at room temperature (cooling with cold water). Next, the 4-bromoacetoacetanilide (3.28 g, 12.8 mmol) was added portionwise over a 20-minute period. The reaction mixture was stirred at 20°-25° C. for 5 hours, filtered under nitrogen atmosphere, and poured into 300 ml of ice-cold water. After acidifying (pH 5-6) with several drops of concentrated hydrochloric acid, the crude product was filtered off and crystallized from ethanol to provide 2.8 g. of amide product, m.p. 182°-184° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04845122 |
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| Quelldatensatz | uspto-grants-1989_07 |
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| ORD ID | ord-727b3696ee3c4956a2b6d68519769f7d |
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| Quellennotiz | uspto-grants-1989_07 |
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