HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 1-Methyl-beta-oxo-alpha-(p-methoxyphenylcarbamoyl)-2-pyrrolpropionitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1-Isocyanato-4-methoxybenzene | HCID 79443 | — |
| Edukt | 3-(1-Methyl-1H-pyrrol-2-yl)-3-oxopropanenitrile | HCID 2777170 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-Methyl-beta-oxo-alpha-(p-methoxyphenylcarbamoyl)-2-pyrrolpropionitrile | HCID 14555704 | — |
Reaktionsschritte
The suspension of 2.0 g of the 1-methyl-β-oxo-2-pyrrolpropionitrile in 50 ml of toluene and 1.6 g of triethylamine is treated with 2.1 g of p-methoxyphenylisocyanate. The mixture is warmed gently until all is dissolved and allowed to stand overnight at room temperature. It is evaporated, the residue is taken up in methanol and combined with 10 ml of 10% aqueous sodium hydroxide and 250 ml of water. The alkaline solution is filtered, acidified with 5 N hydrochloric acid and the precipitate formed collected. It is washed with water, dried, triturated with warm methanol-ethyl acetate, and recrystallized from ethyl acetate, to yield the 1-methyl-β-oxo-α-(p-methoxyphenylcarbamoyl)-2-pyrrolpropionitrile melting at 192°-193°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04256759 |
| Quelldatensatz | uspto-grants-1981_03 |
| ORD ID | ord-bd67a2403f5947ea99ebdfd823a2528c |
| Quellennotiz | uspto-grants-1981_03 |