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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253101Generated: October 26, 2026

Ethyl 5-benzylnicotinate → Ethyl 5-(cyclohexylmethyl)piperidine-3-carboxylate

https://huagongshe.com/reaction/253101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-benzylnicotinateHCID 66610002—
CatalystAdams' catalystHCID 345198—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductEthyl 5-(cyclohexylmethyl)piperidine-3-carboxylateHCID 6684462773%

Reaction Steps

A suspension of ethyl-5-benzylnicotinate (1.0 g, 4.1 mmol) and PtO2 (800 mg) in EtOH (25 mL) and HCl (conc., 5.0 mL) was mixed in a Parr shaker under 40 psi of H2 for 2 hours. The mixture was filtered through celite and concentrated to about 10% of the original volume. The resulting mixture was extracted with CH2Cl2 (3×30 mL). The organic layer was concentrated under reduced pressure to furnish the title compound (755 mg, 73% yield) as a white solid. MS m/z: 254.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-32c156fd940f498890066107f181b7d7
Source noteuspto-grants-2011_01