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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493868Generated: October 31, 2026

N-(1-Benzyl-4-piperidyl)-N-(4-fluorophenyl)-4-fluorobenzamide hydrochloride → HCID 19829436, compound

https://huagongshe.com/reaction/1493868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-Benzyl-4-piperidyl)-N-(4-fluorophenyl)-4-fluorobenzamide hydrochlorideHCID 19829407—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 19829436HCID 1982943690.2%

Reaction Steps

N-(1-Benzyl-4-piperidyl)-N-(4-fluorophenyl)-4-fluorobenzamide hydrochloride (3.2 g) in 95% strength ethanol (50 cc) is hydrogenated at 60° C. at atmospheric pressure in the presence of palladium hydroxide (0.5 g). After filtration through kieselguhr and concentration to dryness under reduced pressure (5.2 kPa), N-(4-fluorophenyl)-N-(4-piperidyl)-4-fluorobenzamide hydrochloride (2.3 g) is obtained in the form of a white powder, m.p. 170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025013
Source datasetuspto-grants-1991_06
ORD IDord-9e2b576f16564775bf533d48dfb79a96
Source noteuspto-grants-1991_06