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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59627Generated: October 28, 2026

Hydrochloric Acid → Sulfentrazone

https://huagongshe.com/reaction/59627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(5-Amino-2,4-dichlorophenyl)-4-(difluoromethyl)-2,4-dihydro-5-methyl-3H-1,2,4-triazol-3-oneHCID 11055966—
CatalystTetrabutylammonium BromideHCID 74236—
ProductSulfentrazoneHCID 86369—

Reaction Steps

The solid 1-(5-amino-2,4-dichlorophenyl)-4,5-dihydro-4-difluoromethyl-3-methyl-1,2,4-triazol-5(1H)-one (1.0 equiv.) was suspended in 20 equivalent of water and the reaction mixture chilled to 10 C. Vigorous stirring was commenced and 0.05 equiv of tetrabutylammonium bromide in 0.05 equiv of toluene was added. Using a pH meter, the of the suspension was brought to 7.8 by adding adequate quantity of 1 molar sodium carbonate aqueous solution. Simultaneous addition of 1.2 equiv methanesulfonyl chloride was started into the reaction while keeping the flow of the aqueous sodium carbonate on such that the pH of 7.8 was maintained throughout. After 45 minutes the reaction was complete and the suspension was replaced by a clear solution. Concentrated hydrochloric acid was added slowly to bring the pH of the reaction to 2.0 wherein a precipitate was formed. The precipitate was collected by filtration, washed with water and dried to give the N-[2,4-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl] phenyl]methanesulfonamide as a white solid (0.96 equiv and 96% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440932B2
Source datasetuspto-grants-2016_09
ORD IDord-3a09bb510bc34a159a754319a649b5f6
Source noteuspto-grants-2016_09