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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257134Generated: November 1, 2026

Hydrochloric Acid → Methyl-phenethyl-piperidin-4-YL-amine

https://huagongshe.com/reaction/2257134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-[N-methyl-N-(2-phenylethyl)amino]-1-benzylpiperidineHCID 1378444—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl-phenethyl-piperidin-4-YL-amineHCID 1085696670.1%

Reaction Steps

60 ml of concentrated hydrochloric acid and 13.3 g of 10% palladium-carbon were added to a solution of 266 g of 4-[N-methyl-N-(2-phenylethyl)amino]-1-benzylpiperidine in 1 liter of ethanol and 500 ml of water. The mixture was stirred at a hydrogen pressure of 1 atm. at 60° C. for 5 hours. 10% palladium-carbon was removed by filtration and then washed with ethanol. The filtrate and the washings were combined and concentrated under reduced pressure. The residue was added to ice water. The mixture was made alkaline with a 25% aqueous sodium hydroxide solution and then extracted with methylene chloride. The extract was water-washed and then concentrated under reduced pressure. The residue was subjected to vacuum distillation to obtain 131.9 g of 4-[N-methyl-N-(2-phenylethyl)amino]piperidine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656642
Source datasetuspto-grants-1997_08
ORD IDord-ccaefee9825b4c4a9a5e209782ff7498
Source noteuspto-grants-1997_08