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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396310Generated: October 29, 2026

Water → 3,5-Diethyl-3-methyl-1-(phenylmethyl)-4-piperidinone

https://huagongshe.com/reaction/396310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
SolventEthyl AcetateHCID 8857—
Product3,5-Diethyl-3-methyl-1-(phenylmethyl)-4-piperidinoneHCID 22278878—

Reaction Steps

1-Benzyl-3-methyl-piperidin-4-one (50 g, 246 mmole) was added to the stirred suspension of sodium hydride (12.0 g, 300.0 mmole) in tetrahydrofuran (500 ml) at ambient temperature and stirring was continued for 1 hr. Ethyl iodide (42.5 ml, 520.0 mmole) in dry tetrahydrofuran (100 ml) was added it at 0-5° C. The resulting mixture stirred at room temperature for 18 hr, water (100 ml) and ethyl acetate (800 ml) were added respectively. Organic layer was separated, dried (Na2SO4) and concentrated to give crude product, which was purified through column chromatography. Elute from 5% ethyl acetate in hexane afforded 1-benzyl-3,5-diethyl-3-methylpiperidin-4-one. Yield 12.0 g (19%), C17H25NO, m/z 260 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-cd8fac6196d04a7a999cf56a9f06cb86
Source noteuspto-grants-2003_08