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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741646Generated: October 30, 2026

Sulfuryl chloride → 4,5-Dichloro-2-[4-(trifluoromethoxy)phenyl]-1,2-thiazol-3(2H)-one

https://huagongshe.com/reaction/741646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantSodium BicarbonateHCID 516892—
Reactant3(2H)-Isothiazolone, 2-[4-(trifluoromethoxy)phenyl]-HCID 9881650—
ReactantHCID 15390069HCID 15390069—
SolventDichloromethaneHCID 6344—
Product4,5-Dichloro-2-[4-(trifluoromethoxy)phenyl]-1,2-thiazol-3(2H)-oneHCID 1539007070.2%

Reaction Steps

First, a mixture containing 6.4 g of 2-(4-trifluorornethoxyphenyl)-4-isothiazolin-3-on and 5.1 g of 2-(4-trifluoromethoxyphenyl)-5-chloro-4-isothiazolin-3-on was suspended in 100 ml of dichloromethane, after which 19 g of sulfuryl chloride was then added dropwise to the suspension dropwise at room temperature, and the resultant mixture was stirred for 12 hours. After completion of the reaction, 200 ml of a saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture, and the dichloromethane layer was separated. The aqueous layer was extracted with 150 ml of dichloromethane. The combined dichloromethane layer was washed with water, dried with magnesium sulfate, and concentrated. The concentrate was purified by column chromatography (hexane: ethyl acetate=6:1) to give 4 g of 2-(4-trifluoromethoxyphenyl)-4,5-dichloro-4-isothiazolin-3-on (compound (13); m.p., 129°-130° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552423
Source datasetuspto-grants-1996_09
ORD IDord-ca520151006e442bb3181e28c04c38b5
Source noteuspto-grants-1996_09