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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303630Generated: November 1, 2026

HCID 18187860, compound → HCID 18187489, compound

https://huagongshe.com/reaction/2303630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18187860HCID 18187860—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 18187489HCID 18187489103.6%

Reaction Steps

The partially purified 1-(benzyloxycarbonyl)-4-(3,3-difluoro-3-phenylprop-1-yl)piperidine (247 mg) was hydrogenated at atmospheric pressure in 95% ethanol (4.0 mL) containing 20% Pd(OH)2/C (60 mg). After 6 h, additional 20% Pd(OH)2/C (32 mg) was added and the hydrogenation was continued for another 16 h. The mixture was filtered and the catalyst was washed with 95% ethanol. Evaporation of the filtrate gave 164 mg of crude 4-(3,3-difluoro-3-phenylprop-1-yl)piperidine as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-e81ed9d4b1964496971c6f37b2c78327
Source noteuspto-grants-2002_08