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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639846Generated: October 26, 2026

Water → Ethyl 2-(1,2,3-benzothiadiazol-7-yl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1639846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactantethyl(2E)-3-(1,2,3-benzothiadiazol-7-yl)acrylateHCID 66720648—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 2-(1,2,3-benzothiadiazol-7-yl)cyclopropanecarboxylateHCID 5933456747.2%

Reaction Steps

To a suspension of 60% sodium hydride (1.34 g, 30.7 mmol) in dimethyl sulfoxide (20 mL) was added a solution of trimethylsulfoxonium iodide (6.76 g, 30.7 mmol) in dimethyl sulfoxide (50 mL) at 0° C., and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added a solution of ethyl(2E)-3-(1,2,3-benzothiadiazol-7-yl)acrylate (6.00 g, 25.6 mmol) in dimethyl sulfoxide (130 mL) at 0° C., and the mixture was stirred at room temperature for 6 hr. Water was added and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/2) to give the title compound (3.00 g, yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110585B2
Source datasetuspto-grants-2012_02
ORD IDord-93e41ad5e5be47a09ee6f4558adb608a
Source noteuspto-grants-2012_02