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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369881Generated: October 29, 2026

HCID 23282592, compound → HCID 23282594, compound

https://huagongshe.com/reaction/369881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23282592HCID 23282592—
CatalystHCID 178502593HCID 178502593—
SolventEthanolHCID 702—
ProductHCID 23282594HCID 2328259457.2%

Reaction Steps

To a solution of 4-(3,4-dimethyl-1-piperazinyl)-1-benzylpiperidine (4.2 g) in ethanol (50 ml) is added 20% palladium hydroxide-carbon (0.4 g), and the mixture is subjected to catalytic hydrogenation at 50° C. under atmospheric pressure. The catalyst is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is evaporated to give 4-(3,4-dimethyl-1-piperazinyl)piperidine (1.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140330
Source datasetuspto-grants-2000_10
ORD IDord-8ab3fcdc4262446a958e9ff38127cb79
Source noteuspto-grants-2000_10