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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556943Generated: October 25, 2026

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

https://huagongshe.com/reaction/556943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3,3-dimethylpiperidin-4-oneHCID 9794413—

Reaction Steps

To a solution of 1-Benzyl-3-methyl-piperidin-4-one (2.03 g, 10 mmol) in THF (10 mL) was added potassium t-Butoxide (1.1 g, 10 mmol) and methyl iodide (0.62 mL, 10 mmol). The solution was then stirred at room temperature for about 72 hours. The reaction was quenched with brine and extracted with ethyl acetate. The combined organic layers were concentrated in vacuo, then purified by flash chromatography on silica gel (35 g SiO2, gradient elution from 100% hexane to 100% ethyl acetate) to yield the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058287B2
Source datasetuspto-grants-2011_11
ORD IDord-054dde9eeaf1466ea4c1481de9e9e565
Source noteuspto-grants-2011_11