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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274510Generated: October 25, 2026

Acetic Acid → 2-(2-Fluoro-4-chloro-5-isopropoxyphenyl)-4-methyl-5-trifluoromethylpyridazin-3-one

https://huagongshe.com/reaction/1274510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethylmalonic AcidHCID 487—
ReactantPiperidineHCID 8082—
Reactant3,3,3-Trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone)HCID 69141430—
SolventPyridineHCID 1049—
Product2-(2-Fluoro-4-chloro-5-isopropoxyphenyl)-4-methyl-5-trifluoromethylpyridazin-3-oneHCID 1108982857.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

Under a stream of nitrogen gas, 0.399 g of 3,3,3-trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone), compound 3-3 was dissolved in 2.4 ml of pyridine at room temperature. To this solution were added 0.133 ml of piperidine and 0.159 g of methylmalonic acid. and the mixture was heated to 70° C. and stirred for 3.5 hours. Then, 2.4 ml of acetic acid was added, and stirring was further continued at 130° C. for 8 hours. The reaction solution was left cooling to room temperature and concentrated under reduced pressure. The residue was diluted with 100 ml of diethyl ether. The diluted solution was washed twice with 20 ml of 3 N hydrochloric acid and once with 30 ml of saturated sodium bicarbonate solution, dried with magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was subjected to column chromatography to give 0.255 g of 2-(2-fluoro-4-chloro-5-isopropoxyphenyl)-4-methyl-5-trifluoromethylpyridazin-3-one, compound 5-2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156891
Source datasetuspto-grants-2000_12
ORD IDord-7b08f96a5c9c4f119f31e4746d8a71b0
Source noteuspto-grants-2000_12