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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971689Generated: October 29, 2026

HCID 70544672, compound → HCID 13192234, compound

https://huagongshe.com/reaction/971689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70544672HCID 70544672—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 13192234HCID 13192234—

Reaction Steps

8.2 g (0.025 mol) of trans-3-hydroxy-4-phenoxy-1-carbobenzyloxy-piperidine are dissolved in 140 ml of methanol and hydrogenated in the presence of 0.8 g of a 5% strength palladium-on-charcoal catalyst under normal pressure and at room temperature. After the absorption of hydrogen has ceased, the catalyst is filtered off by means of diatomaceous earth and the filtrate is evaporated under a water pump vacuum. The crude base crystallies from methanol/ether and gives trans-3-hydroxy-4-phenoxy-piperidine with a melting point of 134°-136°. The neutral fumarate prepared therefrom with fumaric acid crystallises from methanol/ether; melting point 180°-183°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160837
Source datasetuspto-grants-1979_07
ORD IDord-2dd38ed6a54645e78f42dfd2415352c9
Source noteuspto-grants-1979_07