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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851044Generated: October 30, 2026

HCID 13039253, compound → HCID 70481907, compound

https://huagongshe.com/reaction/851044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13039253HCID 13039253—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70481907HCID 70481907—

Reaction Steps

A solution of 8.59 g of trans-4-(4-benzyloxyphenoxy)-1-methyl-3-phenylpiperidine in a mixture of 100 ml of absolute ethanol and 50 ml of tetrahydrofuran is hydrogenated overnight over 5% palladium-on-carbon at room temperature under 45 pounds per square inch of hydrogen. The catalyst is filtered and washed with ethanol and ether. The filtrate is concentrated in vacuo to a nearly colorless, partially solidified foam. Trituration of the foam with ether followed by recrystallization from 270 ml of chloroform gives product as a colorless solid, mps 169.5° C., 170°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382141
Source datasetuspto-grants-1983_05
ORD IDord-a9beea724f0448a5ae7d7214c70a2758
Source noteuspto-grants-1983_05