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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381864Generated: October 25, 2026

Potassium Carbonate → 4-Chloro-5-methoxy-2-phenyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/381864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4,5-Dichloro-2-phenyl-3(2H)-pyridazinoneHCID 72813—
ReactantHCID 18991304HCID 18991304—
SolventMethanolHCID 887—
Product4-Chloro-5-methoxy-2-phenyl-3(2H)-pyridazinoneHCID 34984295%

Reaction Steps

The title compound was prepared according to the method of (S. Cho et al. described in J. Het. Chem., (1996), 33, 1579-1582), starting with the N-phenyl-dichloropyridazinone. A mixture of 2-phenyl-4,5-dichloro-3(2H)-pyridazinone (1 g, 4.1 mmol) and finely powdered, anhydrous K2CO3 (580 mg, 4.2 mmol) in 50 mL of methanol was heated at reflux for 5 hours and concentrated in vacuo. The residue was partitioned between water and ethyl acetate. The acetate layer was washed with water, and brine to provide 2-phenyl-4-chloro-5-methoxy-3(2H)-pyridazinone (yield: 920 mg, 95%). 1H NMR (300 MHz, DMSO-d6) δ 4.15 (s, 3H), 7.50 (m, 5H), 8.43 (s, 1H). MS (DCI/NH3) m/z 237 (M+H)+, 254 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307047B1
Source datasetuspto-grants-2001_10
ORD IDord-926ab51aac9f4bd69fa2bfa9d76580d3
Source noteuspto-grants-2001_10