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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508587Generated: October 25, 2026

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

https://huagongshe.com/reaction/508587

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 numberUS09096533B2
Source datasetuspto-grants-2015_08
ORD IDord-3aa29f9a475447a0b0b1adf0e6cb5ece
Source noteuspto-grants-2015_08