Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421621Generated: October 31, 2026

Sulfuric Acid → 2-(4-Chlorophenyl)-5-trifluoromethylpyridazin-3-one

https://huagongshe.com/reaction/1421621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantHCID 1474610HCID 1474610—
SolventWaterHCID 962—
Product2-(4-Chlorophenyl)-5-trifluoromethylpyridazin-3-oneHCID 1105489745.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

Two mililiters (2 ml) of a mixture of sulfuric acid and water (v/v=1/1), and 0.5 g of 2-(4-chlorophenyl)-6-ethoxycarbonyl-5-trifluoromethylpyridazin-3-one (the present compound 1-51) were mixed and heated for 5 hours on a 150° C. oil bath. The reaction solution was cooled to room temperature, poured into water and extracted with 100 ml of ethyl acetate. The organic layer was washed with 50 ml of saturated sodium chloride solution twice and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the obtained crystals were washed with 50 ml of n-hexane to afford 0.18 g of 2-(4-chlorophenyl)-5-trifluoromethylpyridazin-3-one (yield:45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077953
Source datasetuspto-grants-2000_06
ORD IDord-e754356bbc0344028efcbef956b64108
Source noteuspto-grants-2000_06