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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713656Generated: October 30, 2026

Sodium Thiosulfate → 3-ethylsulfonyl-N-(4-trifluoromethoxyphenyl)picolinamide

https://huagongshe.com/reaction/713656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant3-ethylsulfanyl-N-(4-trifluoromethoxyphenyl)picolinamideHCID 118113332—
SolventChloroformHCID 6212—
Product3-ethylsulfonyl-N-(4-trifluoromethoxyphenyl)picolinamideHCID 118113485—

Reaction Steps

0.84 g of m-chloroperbenzoic acid (purity of 68%) was added to a mixture of 0.50 g of 3-ethylsulfanyl-N-(4-trifluoromethoxyphenyl)picolinamide (Compound of Present Invention 18) and 5 mL of chloroform under ice cooling, and the mixture was stirred at room temperature for 3 hours. A saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium thiosulfate solution were poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.50 g of 3-ethylsulfonyl-N-(4-trifluoromethoxyphenyl)picolinamide (hereinafter, referred to as Compound of Present Invention 21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09185910B2
Source datasetuspto-grants-2015_11
ORD IDord-a489713a0cf84a239daac67dfc7ad884
Source noteuspto-grants-2015_11