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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852561Generated: October 31, 2026

Sodium Carbonate → 4-(2-ethylphenyl)-5-methoxy-2-methyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/1852561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,4-DioxaneHCID 31275—
Reactant4-Chloro-5-methoxy-2-methyl-2,3-dihydropyridazin-3-oneHCID 2774938—
Reactant2-Ethylphenylboronic Acid (contains varying amounts of Anhydride)HCID 4100862—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product4-(2-ethylphenyl)-5-methoxy-2-methyl-3(2H)-pyridazinoneHCID 5743731792%

Reaction Steps

To a mixture of 2.516 g of 4-chloro-5-methoxy-2-methyl-3(2H)-pyridazinone, 2.575 g of 2-ethylphenylboronic acid and 3.333 g of sodium carbonate were added 30 mL of 1,4-dioxane and 20 mL of water. To the mixture were added 2.417 g of tetrabutylammonium bromide and 0.657 g of tetrakis(triphenylphosphine)palladium, and then under a nitrogen atmosphere, the resulting mixture was stirred and heated under reflux for 17 hours. After cooling, 50 mL of water was added to the reaction mixture, which was extracted with 100 mL of ethyl acetate and then 30 mL of ethyl acetate. The extracts were combined, washed with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The solid obtained was washed with a mixed solvent of ethyl acetate and hexane (1:2) to yield 3.238 g of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962625B2
Source datasetuspto-grants-2015_02
ORD IDord-621473a11b2d4179b78775457394402f
Source noteuspto-grants-2015_02