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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675330Generated: October 27, 2026

Water → (3,4-Dichloroisothiazol-5-yl)methyl benzoate

https://huagongshe.com/reaction/1675330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant(3,4-Dichloroisothiazol-5-yl)methanolHCID 16723166—
SolventTolueneHCID 1140—
Product(3,4-Dichloroisothiazol-5-yl)methyl benzoateHCID 2365860487.3%

Reaction Steps

3.0 g (16.3 mmol) of the above-produced (3,4-dichloroisothiazol-5-yl)methanol and 2.52 g (17.9 mmol) of benzoyl chloride were dissolved in 70 ml of toluene. Thereto was dropwise added, under ice-cooling, 1.98 g (19.6 mmol) of triethylamine. The mixture was stirred at room temperature for 3 hours. Water was added, followed by extraction with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated. The resulting crystals were washed with hexane to obtain 4.1 g (yield: 87%) of (3,4-dichloroisothiazol-5-yl)methyl benzoate as colorless crystals (melting point: 79 to 80° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003675B2
Source datasetuspto-grants-2011_08
ORD IDord-eabea0dbe4404a639aeb9a1e478a5cde
Source noteuspto-grants-2011_08