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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973441Generated: October 25, 2026

Potassium Iodide → N-(2-(2-Methyl-5-nitro-1H-imidazol-1-yl)ethyl)phthalimide

https://huagongshe.com/reaction/1973441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
Reactant1-(2-Chloroethyl)-2-methyl-5-nitroimidazoleHCID 83210—
ReactantPhthalimide potassium saltHCID 24194345—
SolventTolueneHCID 1140—
ProductN-(2-(2-Methyl-5-nitro-1H-imidazol-1-yl)ethyl)phthalimideHCID 120116—

Reaction Steps

A mixture of 17.0 parts of 1-(2-chloroethyl)-2-methyl-5-nitroimidazole, 18.0 parts of potassium phthalimide, and 2.0 parts of potassium iodide in 240 parts of dimethylformamide is heated in a boiling water bath for 3 hours with stirring. Stirring is then continued for 16 hours at room temperature. The resulting brown mixture is diluted with 870 parts of toluene and the toluene solution is washed with several portions of water. The toluene solution is dried over sodium sulfate and the solvent is evaporated to leave a residue which is digested with cold alcohol. The alcohol solution is then cooled and the precipitate which forms is separated by filtration and recrystallized from ethanol to give N-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]phthalimide melting at about 177° C. This compound has the following formula ##STR6##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997572
Source datasetuspto-grants-1976_12
ORD IDord-513ccd2c1b85446794e18bd6e223f312
Source noteuspto-grants-1976_12