HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 620922Erstellt: 24. Oktober 2026
Diethylamine → 1-(2,2-Diethoxyethyl)cyclohexane-1-carbonitrile
https://huagongshe.com/de/reaction/620922
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethylamine | HCID 8021 | — |
| Edukt | Cyanocyclohexane | HCID 69834 | — |
| Edukt | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 1-(2,2-Diethoxyethyl)cyclohexane-1-carbonitrile | HCID 13217350 | — |
Reaktionsschritte
51.7 ml (0.5 mol) of anhydrous diethylamine are added dropwise, under protective gas at -10° C., to 312.5 ml (0.5 mol) of a 15% strength solution of n-butyllithium in hexane. The mixture is stirred for 20 minutes and then cooled to -70° C. 54.6 g of cyclohexanecarbonitrile are added dropwise over the course of 30 minutes and, after a further 30 minutes, 98.5 g of bromoacetaldehyde diethyl acetal are added within 1 hour and the mixture is left at low temperature for 24 hours. It is then warmed to room temperature, 100 g of ice are added, and the mixture is extracted twice with 500 ml of ethyl acetate, and the organic phase is dried over sodium sulfate, evaporated in vacuo and the residue is subjected to vacuum distillation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04822894 |
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| Quelldatensatz | uspto-grants-1989_04 |
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| ORD ID | ord-c95d3c5d99e543bf941100058e7e16a4 |
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| Quellennotiz | uspto-grants-1989_04 |
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