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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971683Generated: October 29, 2026

HCID 13192226, compound → HCID 13192228, compound

https://huagongshe.com/reaction/971683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13192226HCID 13192226—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 13192228HCID 13192228—

Reaction Steps

16.0 g (0.04 mol) of trans-3-acetoxy-4-(3,4-dimethyl-phenoxy)-1-carbobenzyloxy-piperidine are dissolved in 400 ml of methanol and hydrogenated in the presence of 1.5 g of a 5% strength palladium-on-charcoal catalyst under normal pressure. After the reaction has ended, the catalyst is filtered off by means of a layer of diatomaceous earth and the filtrate is evaporated under a water pump vacuum, whereupon trans-3-acetoxy-4-(3,4-dimethylphenoxy)-piperidine is obtained in the form of a yellow oil. Reaction of the base with fumaric acid in ethanol/ether gives the crystalline acid fumarate with a melting point of 170°-172°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160837
Source datasetuspto-grants-1979_07
ORD IDord-eb1d45ae8a8a4bbe8e85dbb7e8fca1cd
Source noteuspto-grants-1979_07