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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256035Generated: November 2, 2026

HCID 19029125, compound → 4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine

https://huagongshe.com/reaction/2256035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19029125HCID 19029125—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidineHCID 19029146981.2%

Reaction Steps

A solution of 1-benzyloxycarbonyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine (0.18 g) in ethanol (5 mL) was hydrogenated over 10% palladium on carbon (0.050 g) at a hydrogen pressure of 1 bar for 2 hours. The catalyst was then removed by filtration through diatomaceous earth, the filter cake was washed with ethanol and the solvent evaporated to afford the piperidine as a white crystalline solid (0.98 g); mp 64°-66° C.; NMR (CDCl3): 3.17 (m, 2), 2.98 (m, 1), 2.75 (dr,2, J=2.6, 12.0), 2.51 (s, 3), 2.01 (m, 2), 1.75 (m, 2); MS: m/z=196(M+1+28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654299
Source datasetuspto-grants-1997_08
ORD IDord-e6ce7915afab43cda9ddd22c7cd62fd1
Source noteuspto-grants-1997_08