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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437553Generated: October 28, 2026

HCID 21428729, compound → 3-(4-Methylphenoxy)piperidine

https://huagongshe.com/reaction/437553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21428729HCID 21428729—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(4-Methylphenoxy)piperidineHCID 21428718—

Reaction Steps

A solution of 2.9 g of 1-benzyl-3-(p-tolyloxy) piperidine in 30 ml. of 95% ethanol is added to 0.42 g of 10% Pd-C, and hydrogenated at about 50° C. for 3 hours. Then the reaction mixture is cooled to ambient temperature, the 10% Pd-C is filtered off, and the ethanol is removed leaving a yellow oil of 3-(p-tolyloxy)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031221
Source datasetuspto-grants-1977_06
ORD IDord-bcc6ccc6d8834f7590a0d0ef152c2668
Source noteuspto-grants-1977_06