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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247110Generated: October 25, 2026

Piperidine → 5-Acetonyl-3-piperidinomethyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/247110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
Reactant5-Acetonyl-3-chloromethyl-1,2,4-oxadiazoleHCID 13824705—
SolventTetrahydrofuranHCID 8028—
Product5-Acetonyl-3-piperidinomethyl-1,2,4-oxadiazoleHCID 1382470656.8%

Reaction Steps

To a solution of 15.0 g of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole in 50 ml of THF were added dropwise 17.4 g of triethylamine and subsequently 11.0 g of piperidine. The mixture was stirred at room temperature for 24 hours and then heated under reflux for 6 hours. After cooling, the precipitated material was removed by filtration and the filtrate was evaporated in vacuo. The residue was chromatographed on silica gel using chloroform-methanol (20:1, v/v) as eluent to give 10.9 g of 5-acetonyl-3-piperidinomethyl-1,2,4-oxadiazole as a colorless solid, m.p. 66°-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705786
Source datasetuspto-grants-1987_11
ORD IDord-424a10afc27f4ca58e6791c1a2642d37
Source noteuspto-grants-1987_11