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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2802Generated: October 23, 2026

Methyl iodide → 4-Bromo-1,3,5-trimethylpyrazole

https://huagongshe.com/en/reaction/2802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-bromo-3,5-dimethyl-1H-pyrazoleHCID 76937—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
Product4-Bromo-1,3,5-trimethylpyrazoleHCID 519181—

Reaction Steps

4-Bromo-3,5-dimethylpyrazole (10 g) in dry dimethylformamide (50 ml) was added to a stirred suspension of sodium hydride (1.8 g) in dry dimethylformamide at 0° C. When the evolution of hydrogen was complete, iodomethane (8.9 g) was added dropwise. The mixture was allowed to warm to room temperature and after 30 minutes saturated aqueous sodium hydrogen carbonate (5 ml) was added. Following evaporation under high vacuum, the residue was purified by column chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731335
Source datasetuspto-grants-1998_03
ORD IDord-ac7f5eb35ef547d1a557dea38319f19e
Source noteuspto-grants-1998_03