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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707598Generated: October 30, 2026

Methyl iodide → 1,3,4-Trimethylpyridin-1-ium iodide

https://huagongshe.com/reaction/1707598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant3,4-DimethylpyridineHCID 11417—
SolventAcetoneHCID 180—
Product1,3,4-Trimethylpyridin-1-ium iodideHCID 12543166—

Reaction Steps

As shown in Scheme 2 (in FIG. 2), a solution of 100 g of 3,4-dimethylpyridine in 800 ml of acetone was added dropwise to 57.27 mL of methyl iodide. The reaction mixture was stirred at room temperature for 18 hrs. The solid was collected by filtration and washed with cold ether. After drying under vacuum, there was obtained 202 g of 1,3,4-trimethylpyridinium iodide. The subsequent Grignard reaction was conducted under standard conditions to afford an unstable intermediate that was utilized immediately.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354758
Source datasetuspto-grants-1994_10
ORD IDord-ce38c26ff9634aa1870c0c0115da3771
Source noteuspto-grants-1994_10