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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092948Generated: October 31, 2026

Chlorosulfonic acid → HCID 42633764, compound

https://huagongshe.com/reaction/2092948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 42633763HCID 42633763—
SolventEthyl AcetateHCID 8857—
ProductHCID 42633764HCID 4263376499%

Reaction Conditions

Temperature70 °C

Reaction Steps

In a 25-ml eggplant flask provided with a magnetic stirrer were placed 2.5 g (22 mol) of chlorosulfonic acid and then 1.8 g (7.4 mmol) of 1,3-dimethyl-4-(3-trifluoromethyl-1H-1,2,4-triazol-1-yl)benzene. The mixture was stirred at 70° C. for 2 hours. The mixture was cooled to room temperature and then added onto ice in small portions. Thereto was added 30 ml of ethyl acetate to give rise to phase separation. The aqueous phase was extracted with 30 ml of ethyl acetate. The ethyl acetate phase was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. Then, vacuum distillation was conducted to distill off ethyl acetate to obtain a title compound as 2.5 g of brown oil. Yield: 99%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440838B2
Source datasetuspto-grants-2013_05
ORD IDord-a00cc8b01ee4477ab134f0c7b1ab7bc3
Source noteuspto-grants-2013_05