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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108198Generated: October 26, 2026

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

https://huagongshe.com/reaction/2108198

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 ml), 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 numberUS04937346
Source datasetuspto-grants-1990_06
ORD IDord-83fd337615f346a491b3820685672f3d
Source noteuspto-grants-1990_06