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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573402Generated: October 25, 2026

Hydrogen Peroxide → HCID 178510672, compound

https://huagongshe.com/reaction/573402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSulfuric AcidHCID 1118—
ReactantFipronil sulfideHCID 9953940—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 178510672HCID 17851067274.4%

Reaction Conditions

Temperature13.5 °C

Reaction Steps

1.5 liter of ethylene dichloride & 421.0 gms of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluromethylphenyl)-4-trifluromethylthio pyrazole was charged in a reactor flask with overhead stirring & condenser system. This mass was then cooled to 12-15° C. and 68.0 gms of H2O2 (50.0% w/w) & 500.0 gms of H2SO4 (90.0% w/w) were simultaneously added over a period of 3.0 to 4.0 hours. The reaction temperature was then raised to 28-30° C. & maintained for about 2.0 hours. The reaction mass obtained thereafter was slowly added into 1700 ml of chilled water at 10-20° C. over a period of 2.0 hours. To this mass, 1500 ml of ethylene dichloride was added and the mixture was heated to 60° C. in order to separate the aqueous and organic layers. The obtained organic phase was washed with water & then with 5% NaHCO3 solution followed by water wash, till a neutral pH was obtained. The crude yield of fipronil after removal of solvent was 425.0 gms. The crude fipronil was crystallized from same solvent after partial evaporation to yield 325 gms of crystalline fipronil with 94.0% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029564B2
Source datasetuspto-grants-2015_05
ORD IDord-3b92c559105a4e73a0c126c59e1d6765
Source noteuspto-grants-2015_05