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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413781Generated: November 2, 2026

(-)-N-benzyl-3-(3-methoxyphenyl)piperidine hydrochloride → 3-(3-Methoxyphenyl)piperidine hydrochloride

https://huagongshe.com/reaction/2413781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(-)-N-benzyl-3-(3-methoxyphenyl)piperidine hydrochlorideHCID 23045634—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(3-Methoxyphenyl)piperidine hydrochlorideHCID 19987255—

Reaction Steps

(-)-N-benzyl-3-(3-methoxyphenyl)piperidine hydrochloride (3.8 g, 0.0120 mol) was dissolved in ethanol (80 m), 10% Pd/C was added and the mixture was hydrogenated at room temperature and atmospheric pressure (28 h). The catalyst was removed (Celite) by filtration, the solvent was evaporated off and the crystalline residue was recrystallized from methanol-ether giving the desired (+)-3-(3-methoxyphenyl)-piperidine hydrochloride (2.54 g, 30% total yield of the maximal theoretical) m.p. 175.5°-177° C.; [α]22D +10.1° (C 2.1, CH3OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719219
Source datasetuspto-grants-1988_01
ORD IDord-bd1ca54b6080438583827054391083e0
Source noteuspto-grants-1988_01