Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682163Generated: November 1, 2026

Diethylamine → 1-(2,2-Diethoxyethyl)cyclohexane-1-carbonitrile

https://huagongshe.com/reaction/1682163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantCyanocyclohexaneHCID 69834—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
Product1-(2,2-Diethoxyethyl)cyclohexane-1-carbonitrileHCID 13217350—

Reaction Conditions

Temperature-70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175306
Source datasetuspto-grants-1992_12
ORD IDord-7b802bb3bfd4452cac497edaa52dc315
Source noteuspto-grants-1992_12