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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59628Generated: October 28, 2026

Hydrochloric Acid → Sulfentrazone

https://huagongshe.com/reaction/59628

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.) and 1.2 equiv of methanesulfonyl chloride 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 pH of the suspension was brought to 7.8 by adding adequate quantity of 1 molar sodium carbonate aqueous solution and dynamically maintained for 1 hour. The suspension was much reduced but not eliminated. 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 (0.41 equiv and 91% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440932B2
Source datasetuspto-grants-2016_09
ORD IDord-7f3a77659be346f980d09e4c1cbfc8db
Source noteuspto-grants-2016_09