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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242559Generated: October 24, 2026

Methyl iodide → 1-Benzyl-3,5-dimethylpiperidin-4-one

https://huagongshe.com/en/reaction/242559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3,5-dimethylpiperidin-4-oneHCID 22278920—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To 1-benzyl-3-methyl-4-piperidone (2.0 g, 9.8 mmol) in THF at about −78° C. under argon, was added Lithium diisopropylamide (7.35 mL, 14.7 mmol, 2 M in heptane/THF/ethylbenzene). After stirring for about 1 hour at about −78° C., iodomethane (0.73 mL, 11.8 mmol) was added. The reaction mixture was stirred for about 1 hour at about −78° C., then warmed to room temperature. Stirring was continued overnight at room temperature. The reaction was quenched with saturated ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with water, then brine and dried over magnesium sulfate. The crude product was chromatographed on silica gel, eluting with EtOAc/hexane (3:10) to give a yellow oil of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-d139616e329d44ceabb8a5c420ff567d
Source noteuspto-grants-2014_02