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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977939Generated: October 26, 2026

Iodoethane → 1-Ethylpiperidine-2,4-dione

https://huagongshe.com/reaction/977939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant4-methoxy-5,6-dihydro-2(1H)-pyridoneHCID 13606575—
SolventDimethylformamideHCID 6228—
Product1-Ethylpiperidine-2,4-dioneHCID 1378411978%

Reaction Steps

Sodium hydride (in the form of a 60% dispersion in oil) (447 mg) is suspended in N,N-dimethylformamide (10 ml), and thereto is added dropwise a solution of 4-methoxy-5,6-dihydro-2(1H)-pyridone (1.29 g) in N,N-dimethylformamide (30 ml). The mixture is stirred under ice-cooling for 30 minutes, and thereto is added dropwise ethyl iodide (0.97 ml). The mixture is stirred under ice-cooling for 30 minutes and further at room temperature for 2.5 hours. The reaction mixture is poured onto water and extracted with chloroform. The extract is washed with a saturated sodium chloride solution and dried. After evaporating the solvent, the residue is dissolved in ethanol (120 ml) and thereto is added 10% hydrochloric acid (60 ml), and the mixture is allowed to stand at 25° C. for 5 hours. After distilling off the solvent under reduced pressure, the residue is dissolved in chloroform, washed with 5% aqueous sodium hydrogen carbonate solution and water, and then dried. The solvent is distilled off to give 1-ethyl-2,4-dioxopiperidine (1.12 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663319
Source datasetuspto-grants-1987_05
ORD IDord-1b9f5830a6bd4b39b57e6d77b7a6a882
Source noteuspto-grants-1987_05