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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283522Generated: October 30, 2026

Cyclohexanone → 1-(Dimethylamino)cyclohexanecarbonitrile

https://huagongshe.com/reaction/1283522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantPotassium CyanideHCID 9032—
ReactantDimethylazanium;chlorideHCID 12954980—
SolventWaterHCID 962—
Product1-(Dimethylamino)cyclohexanecarbonitrileHCID 101188—

Reaction Steps

Dimethylammonium chloride (81.5 g, 1.0 mole) dissolved in water (150 ml.) was added to cyclohexanone (98.0 g., 1.0 mole), quickly followed by a solution of potassium cyanide (68.0 g, 1.045 mole) in water (150 ml.) added over a period of five minutes. The reaction mixture was stirred for 24 hours during which time a colourless crystalline solid was formed. The solid was filtered off, washed with ice cold water (200 ml.), dissolved in benzene (150 ml.) and rewashed with water (100 ml.). The aqueous layer was extracted with benzene (100 ml.), the benzene solutions then being combined, dried over anhydrous sodium sulphate and evaporated under reduced pressure. The oily residue (144 g.) solidified to give 1-cyanocyclohexyldimethylamine, m.p. 36°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975443
Source datasetuspto-grants-1976_08
ORD IDord-20a0031414594075b0c6bb861b071e41
Source noteuspto-grants-1976_08