Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270211Generated: October 30, 2026

Methyl iodide → HCID 21964391, compound

https://huagongshe.com/reaction/270211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 21964343HCID 21964343—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21964391HCID 21964391—

Reaction Steps

A solution of 1-benzyl-3-(3-chlorophenyl)-4-piperidone (75 mmol) in anhydrous THF (250 mL) is cooled to −30° C., then treated with a solution of freshly prepared lithium diisopropylamide (2.0 M in THF/heptane, 45 mL). After stirring for 15 min, a solution of methyl iodide (80 mmol) in THF (40 mL) is rapidly added. The mixture is then stirred for 1 hour at −30° C., warmed quickly to room temperature, and quenched with a saturated aqueous solution of ammonium chloride. The organic layer is collected, washed with water, brine, and dried (MgSO4). After filtering, the filtrate is concentrated in vacuo to afford the desired intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449490B2
Source datasetuspto-grants-2008_11
ORD IDord-76df91655ec24c6f9bf748ea61ac8447
Source noteuspto-grants-2008_11