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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57850Generated: October 25, 2026

Methyl iodide → 5-Chloro-2-methylpyridazin-3(2H)-one

https://huagongshe.com/reaction/57850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloropyridazin-3(2H)-oneHCID 19905718—
SolventDimethylformamideHCID 6228—
Product5-Chloro-2-methylpyridazin-3(2H)-oneHCID 12910144—

Reaction Steps

A solution of 4-chloro-1H-pyridazin-6-one (6.000 mmol; 783.2 mg), Iodomethane (7.200 mmol; 1032 mg; 0.453 mL), and potassium carbonate (9.000 mmol; 1256 mg) in DMF (12 mL) was stirred at room temperature overnight. The mixture was filtered. The filtrate was partitioned between EtOAc and water. The organic layer was concentrated. The residue was purified on silica eluted with 0 to 40% EtOAc in DCM to afford 5-chloro-2-methyl-pyridazin-3-one as an off-white solid (514.7, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434725B2
Source datasetuspto-grants-2016_09
ORD IDord-629f6a2a648d414ab2141a7d9626c816
Source noteuspto-grants-2016_09