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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453878Generated: October 31, 2026

Hydrochloric Acid → 1-Benzyl-4-(dimethylamino)piperidine-4-carbonitrile

https://huagongshe.com/reaction/453878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylamineHCID 674—
ReactantPotassium CyanideHCID 9032—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant1-Benzyl-4-piperidoneHCID 19220—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventEthyl acetate hexaneHCID 21226206—
Product1-Benzyl-4-(dimethylamino)piperidine-4-carbonitrileHCID 1645391585%

Reaction Conditions

Temperature0 °C

Reaction Steps

208 g (3 eq.) N,N-dimethylamine hydrochloride, 154 g (3 eq.) potassium cyanide in 154 ml water and 1050 ml (7 eq.) of a 40% dimethylamine solution were added to a solution of 150 g (1 eq.) 1-benzylpiperidin-4-one in 300 ml methanol and the mixture was cooled to 0° C. 75 ml (0.5 eq.) concentrated hydrochloric acid were then added at 0° C. and the reaction mixture was stirred for 24 h at room temperature. The reaction course was monitored by thin-layer chromatography (20% EtOAc/hexane). Once the conversion was complete, the solid that had formed was filtered out and washed with iced water (4 l). The solid obtained was then dissolved in ethyl acetate and dried with Na2SO4. Following removal of the solvent under reduced pressure, 165 g (85%) of crude product were obtained in the form of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492559B2
Source datasetuspto-grants-2013_07
ORD IDord-71c4587b6e154fcabce253f94ad4d974
Source noteuspto-grants-2013_07