HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 462511Erstellt: 25. Oktober 2026
Diethylamine → 1-(2,2-Diethoxyethyl)cyclohexane-1-carbonitrile
https://huagongshe.com/reaction/462511
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 to 312.5 ml (0.5 mol) of a 15% solution of n-butyl-lithium in hexane at -10° C. under an inert gas blanket. The batch is stirred for 10 minutes and then cooled to -70° C. Within 30 minutes, 54.6 g of cyclohexane-carbonitrile are added dropwise, after a further 30 minutes 98.5 g of bromoacetaldehyde-diethylacetal are added within 1 hour, and the batch is maintained for 24 hours at low temperature. Subsequently, it is warmed to room temperature, given onto 100 g of ice, extracted twice with 500 ml of ethyl acetate, the organic phase is dried over sodium sulfate, concentrated in vacuo, and the residue is subjected to vacuum distillation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04515960 |
|---|
| Quelldatensatz | uspto-grants-1985_05 |
|---|
| ORD ID | ord-26fc452980d64f33bffc69f7d14a2f3a |
|---|
| Quellennotiz | uspto-grants-1985_05 |
|---|