HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127594Erstellt: 26. Oktober 2026
Triethylamine → 1-Methyl-beta-oxo-alpha-(p-nitrophenylcarbamoyl)-2-pyrrolpropionitrile
https://huagongshe.com/reaction/127594
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Benzene, 1-isocyanato-4-nitro- | HCID 66012 | — |
| Edukt | 3-(1-Methyl-1H-pyrrol-2-yl)-3-oxopropanenitrile | HCID 2777170 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-Methyl-beta-oxo-alpha-(p-nitrophenylcarbamoyl)-2-pyrrolpropionitrile | HCID 20285405 | — |
Reaktionsschritte
The solution of 4.9 g of the 1-methyl-β-oxo-2-pyrrolpropionitrile in 50 ml of toluene, 5 ml of dimethylsulfoxide and 4 g of triethylamine is treated with the solution of 5.7 g of p-nitrophenylisocyanate in the minimum amount of toluene while stirring. After standing overnight it is evaporated and the residue taken up in methanol. The solution is filtered, diluted with water and 6 ml of triethylamine, washed with ethyl acetate, and the washings extracted once with 5% aqueous sodium hydroxide. The combined aqueous solutions are acidified with 5 N hydrochloric acid and the precipitate collected. It is washed with water, triturated with methanol-ethanol and recrystallized from dimethylformamide, to yield the 1-methyl-β-oxo-α-(p-nitrophenylcarbamoyl)-2-pyrrolpropionitrile melting at 245°-250° with decomposition.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04256759 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-4724d9ac5eb64a77a9945cca3c2ce5fa |
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| Quellennotiz | uspto-grants-1981_03 |
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