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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054826Generated: October 31, 2026

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

https://huagongshe.com/reaction/2054826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3,5-dimethylpiperidin-4-oneHCID 2227892031.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. solution of 1-benzyl-3-methyl-piperidin-4-one (4.06 g, 20 mmol) in anhydrous THF (20 mL) was added lithium hexamethyldisilazide (21 mL, 21 mmol of a 1.0 M solution THF). After being stirred at −78° C. for 30 min, a solution of iodomethane (1.31 mL, 21 mmol) in THF (5 mL) was added into the reaction mixture. The resultant solution was stirred at 25° C. for 2 h and quenched with water. The aqueous layer was extracted with CH2Cl2. The organic extracts were combined, washed with brine and dried over MgSO4. The solution was filtered and concentrated in vacuo to give the crude product. The crude material was purified by flash column chromatography (hexane/EtOAc) to provide 1.37 g (31.5% yield) of 1-benzyl-3,5-dimethyl-piperidin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329755B2
Source datasetuspto-grants-2008_02
ORD IDord-9dec18361d6d4fbf967c21ce942e8a33
Source noteuspto-grants-2008_02