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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093086Generated: November 2, 2026

Triethylamine → Ethyl 4-oxo-1-piperidinecarboxylate

https://huagongshe.com/reaction/2093086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantPiperidin-2-one--hydrogen chloride (1/1)HCID 20088740—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—

Reaction Steps

To a solution of a piperidone hydrochloride (1 eq) in dichloromethane was added Et3N (2.1 eq) at 0° C. and the reaction mixture was stirred for 15 min. A solution ethyl chloroformate (1.1 eq) in chloroform was added at 0° C. and reaction was continued at room temperature for 3 h Reaction was quenched with water and extracted with ethyl acetate, organic layer was separated, dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford crude product, which, on purification by column chromatography afforded the desired ethyl 4-oxopiperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440830B2
Source datasetuspto-grants-2013_05
ORD IDord-0e613af0ef2144679d6c12fc7a0799a7
Source noteuspto-grants-2013_05