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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236116Generated: October 26, 2026

Water → Dichlobentiazox

https://huagongshe.com/reaction/2236116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantPseudosaccharin chlorideHCID 64783—
Reactant(3,4-Dichloroisothiazol-5-yl)methanolHCID 16723166—
SolventAcetonitrileHCID 6342—
ProductDichlobentiazoxHCID 1775662482.2%

Reaction Steps

In 6 ml of acetonitrile were dissolved 0.62 g (3.10 mmol) of 3-chloro-1,2-benzoisothiazole 1,1-dioxide and 0.57 g (3.10 mmol) of the (3,4-dichloroisothiazol-5-yl)methanol. To the resulting solution was dropwise added 0.34 g (3.4 mmol) of triethylamine, followed by stirring at room temperature for 5 hours to give rise to a reaction. After the completion of the reaction, 12 ml of water was added. The resulting crystals were obtained by filtration. The crystals were washed with water and isopropyl alcohol to obtain 0.89 g (yield: 82%) of 3-(3,4-dichloroisothiazol-5-ylmethoxy)-1,2-benzoisothiazole 1,1-dioxide as a colorless powder (melting point: 165 to 167° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714140B2
Source datasetuspto-grants-2010_05
ORD IDord-87cfdb9d30a44fab894dfce451049edf
Source noteuspto-grants-2010_05