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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437575Generated: October 29, 2026

1-Benzyl-4-(p-trifluoromethylphenoxy)piperidine → 4-(4-(Trifluoromethyl)phenoxy)piperidine

https://huagongshe.com/reaction/437575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(p-trifluoromethylphenoxy)piperidineHCID 12999580—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(4-(Trifluoromethyl)phenoxy)piperidineHCID 3688392—

Reaction Steps

A solution of 46.0 g of 1-benzyl-4-(p-trifluoromethylphenoxy)piperidine, the free base of Part (a), in 250 ml. of 95% ethanol is treated with 6.0 g of 10% palladium-on-charcoal catalyst and is shaken with hydrogen gas at 50° C. until the theoretical amount of hydrogen is absorbed. The suspension is cooled, filtered, and the solvent is removed. The residual oil is fractionally distilled under reduced pressure and the fraction which boils at 74°-76° C/0.05 mm is collected. The collected oil crystallizes on standing to give a solid of 4-(p-trifluoromethylphenoxy)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031221
Source datasetuspto-grants-1977_06
ORD IDord-4ede845a94284a8cbb7621fc786f6722
Source noteuspto-grants-1977_06