Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413778Generated: November 1, 2026

Hydrochloric Acid → 3-(3-Methoxyphenyl)piperidine

https://huagongshe.com/reaction/2413778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant3-(Phenoxymethyl)pyridineHCID 12474431—
CatalystAdams' catalystHCID 345198—
Product3-(3-Methoxyphenyl)piperidineHCID 11074230—

Reaction Steps

To a solution of 3-(3-pyridinyl)methoxybenzene (22.0 g, 0.099 mol) in methanol (250 ml), PtO2 (2 g) and conc. HCl (30 ml) were added and the mixture was hydrogenated at 0.34 MPa in a Parr apparatus. After complete hydrogenation, the catalyst was filtered off. Most of the solvent was evaporated, the residue was made alkaline with 1 M NaOH and extracted with ether. The ether-phase was dried (Na2SO4) and the solvent evaporated giving 18 g of the amine product. The hydrochloride was made and then recrystallized from ethanol/ether yielding 20.9 g (93%), mp. 137°-138.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719219
Source datasetuspto-grants-1988_01
ORD IDord-0bf29e412ba34ef9bb4bbc4a0fa372b0
Source noteuspto-grants-1988_01