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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803800Generated: November 5, 2026

Potassium Chloride → HCID 178510672, compound

https://huagongshe.com/reaction/1803800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ChlorideHCID 4873—
ReactantEthylbenzeneHCID 7500—
ReactantThionyl ChlorideHCID 24386—
ReactantN,N-DimethylisopropylamineHCID 70452—
ReactantTrifluoromethanesulfinic acidHCID 596718—
Reactant5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrileHCID 3303913—
Reactant65476-73-5HCID 18981358—
ProductHCID 178510672HCID 178510672—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 500 ml jacketed reactor with stirrer, baffles and condenser was initially charged under a nitrogen atmosphere with 103 g of ethylbenzene, 6.3 g of dimethylisopropylamine hydrochloride (0.050 mol, 99%) and 15.5 g of potassium chloride (0.208 mmol). Subsequently, 31.5 g of trifluoromethanesulfinic acid (0.223 mol, 95.0%), 17.9 g of dimethylisopropylamine (0.203 mol, 99%) and 24.2 g of thionyl chloride (203 mmol, 99.7%) were metered in at 0° C. with cooling. After subsequently adding 54.8 g of 5-amino-3-cyano-1-(2,6-dichlor-4-trifluoromethylphenyl)pyrazole, the reaction mixture was stirred at 0° C. for 1 h, then heated to 35° C. over 45 min and stirred at 35° C. for a further 10 h. After the reaction had been quenched with sodium hydroxide solution and extracted with ethyl acetate and ethylbenzene, a nonisolated yield of fipronil of 80% was obtained in the crude solution (determination by means of quantitative HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354007B2
Source datasetuspto-grants-2013_01
ORD IDord-e423f6abb02d4fbc8e741ff52e893723
Source noteuspto-grants-2013_01