HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1194546Erstellt: 26. Oktober 2026
Water → diethyl N-(4-ethylcyclohexen-1-yl)-aminomethylenemalonate
https://huagongshe.com/reaction/1194546
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 4-Ethylcyclohexanone | HCID 79506 | — |
| Edukt | Diethyl (aminomethylidene)propanedioate | HCID 226751 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | diethyl N-(4-ethylcyclohexen-1-yl)-aminomethylenemalonate | HCID 14153004 | — |
Reaktionsschritte
A mixture of 12.6 g of 4-ethylcyclohexanone, 17.0 g of diethyl aminomethylenemalonate, and 950 mg of p-toluenesulfonic acid in 170 ml of toluene is heated at reflux for 48 hours with a water separator, under nitrogen atmosphere. The solvent is removed under nitrogen atmosphere and under vacuum, and the residue purified by flash column chromatography on a silica gel column eluted with methylene chloride. The desired product, diethyl N-(4-ethylcyclohexen-1-yl)-aminomethylenemalonate is obtained as an oil. The purified product in 90 ml Dowtherm is added to 300 ml Dowtherm preheated to 250° under nitrogen atmosphere. After heatinq at 240°-245° for 4 hours the reaction mixture is cooled and allowed to stand at room temperature overnight. The precipitate which formed is filtered off, washed with hexane and air-dried. Recrystallization form isopropanol after treatment with decolorizing carbon affords ethyl 4-hydroxy-6-ethyl-5,6,7,8-tetrahydroquinoline-3-carboxylate m.p. 218°-220°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04814450 |
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| Quelldatensatz | uspto-grants-1989_03 |
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| ORD ID | ord-26ddcc76f4274eb9a83f1e918902cb60 |
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| Quellennotiz | uspto-grants-1989_03 |
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