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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537739Generated: October 29, 2026

HCID 57496385, compound → HCID 57496421, compound

https://huagongshe.com/reaction/537739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57496385HCID 57496385—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 57496421HCID 57496421—

Reaction Steps

Benzyl 2-cyclohexyl-4-phenylpiperidine-1-carboxylate (1.05 g, 2.78 mmol) in EtOH (50 ml) was added Pd/C (0.5 g, 0.235 mmol) and hydrogenated with a balloon overnight. Filtered through celite and concentrated. The trans isomer was removed on the chiral OD column 20% IPA/Hexanes w/DEA affording the single cis diastereomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865701B2
Source datasetuspto-grants-2014_10
ORD IDord-4310c8dc9c3a4f1682a3a0a664705109
Source noteuspto-grants-2014_10