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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349382Generated: November 1, 2026

Dimethylamine → 4-Benzyloxy-1-dimethylaminocyclohexanecarbonitrile

https://huagongshe.com/reaction/1349382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantPotassium CyanideHCID 9032—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant4-(Benzyloxy)cyclohexanoneHCID 10987369—
SolventMethanolHCID 887—
Product4-Benzyloxy-1-dimethylaminocyclohexanecarbonitrileHCID 21093240—

Reaction Steps

A mixture of 130 ml of 7.9 molar aqueous dimethylamine solution, 16 ml of methanol, 20.0 g of 4-benzyloxycyclohexanone, 23.2 g of dimethylamine hydrochloride and 15.3 g of potassium cyanide was stirred for 65 hours at room temperature; extraction was carried out four times using 120 ml of diethyl ether each time, and the combined extracts were concentrated; 100 ml of dichloromethane were added to the residue, the phases were separated, and the organic phases were dried over sodium sulfate, filtered and concentrated. 24.5 g of 4-benzyloxy-1-dimethylaminocyclohexanecarbonitrile were obtained in the form of a yellowish oil which slowly solidified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211694B2
Source datasetuspto-grants-2007_05
ORD IDord-4c61180a1d2c49dba50468e13509358b
Source noteuspto-grants-2007_05