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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980872Generated: October 30, 2026

Methyl iodide → 1-Benzyl-3-methyl-4-piperidone

https://huagongshe.com/reaction/980872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3-methyl-4-piperidoneHCID 56096539.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

At first, 4.2 g of 60% sodium hydride was suspended in 200 ml of tetrahydrofuran, and then a solution of 18.9 g of 1-benzyl-4-piperidone and 17.9 g of methyl iodide dissolved in 20 ml of tetrahydrofuran was added dropwise to the suspension at room temperature over 5 minutes. Thereafter, the mixture was heated to 60° C. and stirred for 5 hours. Thereafter, the reaction mixture was filtered. The filtrate was concentrated, and then the concentrate was poured into 150 ml of water and extracted with 120 ml portions of ethyl acetate three times. The extract was washed with 150 ml of brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 21.6 g of an oily matter. The oily matter was purified by silica gel column chromatography (eluent: n-hexane:ethyl acetate=2:1 V/V) to obtain 8.0 g of 1-benzyl-3-methyl-4-piperidone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639522
Source datasetuspto-grants-1987_01
ORD IDord-e6ee90eb5bee4a0b9be8c8a2ce183781
Source noteuspto-grants-1987_01