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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979052Generated: October 25, 2026

Potassium Iodide → 1,3-dimethyl-4-nitro-1H-pyrazole-5-carbonitrile

https://huagongshe.com/reaction/979052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CyanideHCID 9032—
Reactant5-Chloro-1,3-dimethyl-4-nitro-1H-pyrazoleHCID 279515—
SolventAcetonitrileHCID 6342—
Product1,3-dimethyl-4-nitro-1H-pyrazole-5-carbonitrileHCID 96507—

Reaction Steps

Fifty-five g of 1,3-dimethyl-4-nitro-5-chloropyrazole was dissolved in 400 ml acetonitrile and 17.45 g potassium cyanide added, followed by 0.5 g potassium iodide and 5 ml DMF. The mixture was refluxed for 22 hours, then cooled, and filtered. The filtrate was concentrated under reduced pressure, then added to stirred water. The resulting percipitate was collected, dried, and recyrstallized in isopropanol. mp, 85°-87° C. A second recrystallization again in ethanol gave the product having increased purity, mp 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04666908
Source datasetuspto-grants-1987_05
ORD IDord-02e5eba2d86747a6ad61fc9c271d97c8
Source noteuspto-grants-1987_05