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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052936Generated: November 2, 2026

Sodium Thiosulfate → HCID 72944737, compound

https://huagongshe.com/reaction/1052936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 118035682HCID 118035682—
SolventChloroformHCID 6212—
ProductHCID 72944737HCID 72944737—

Reaction Steps

0.82 g of m-chloroperbenzoic acid (purity of 68%) was added to a mixture of 0.63 g of 2-ethylsulfanyl-N-methyl-4-trifluoromethyl-N-(5-trifluoromethylsulfanyl-pyridin-2-yl)-benzamide and 10 mL of chloroform under ice cooling, and the mixture was stirred for 2 hours under ice cooling. A saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium thiosulfate solution were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.62 g of 2-ethylsulfonyl-N-methyl-4-trifluoromethyl-N-(5-trifluoromethylsulfanyl-pyridin-2-yl)-benzamide (hereinafter, referred to as Compound of Present Invention 10) and 0.04 g of 2-ethylsulfonyl-N-methyl-4-trifluoromethyl-N-(5-trifluoromethylsulfinyl-pyridin-2-yl)-benzamide (hereinafter, referred to as Compound of Present Invention 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09392791B2
Source datasetuspto-grants-2016_07
ORD IDord-d67ac46e8fc045baa7cb6ff3510ce1e1
Source noteuspto-grants-2016_07