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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396335Generated: October 29, 2026

Water → 1-Benzyl-3,5-dimethyl-3-ethyl-4-piperidone

https://huagongshe.com/reaction/396335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzyl-3-ethylpiperidin-4-oneHCID 6490960—
SolventEthyl AcetateHCID 8857—
Product1-Benzyl-3,5-dimethyl-3-ethyl-4-piperidoneHCID 22278897—

Reaction Steps

1-Benzyl-3-ethyl-piperidin-4-one (33 g, 152.0 mmole) was added to the stirred suspension of sodium hydride (9.5 g, 200.0 mmole) in tetrahydrofuran (300 ml) at 32° C. and stirring was continued for 1 hr. Methyl iodide (30 ml, 490.0 mmole) in dry tetrahydrofuran (100 ml) was added it at 0-5° C. The resulting mixture stirred at room temperature for 4 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 10% ethyl acetate in hexane afforded 1-benzyl-3,5-dimethyl-3-ethylpiperidin-4-one. Yield 22.0 g (59%), C16H23NO, m/z 246 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-fa84d4909e204876ada75d2f233342d8
Source noteuspto-grants-2003_08