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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300028Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 18374274, compound

https://huagongshe.com/reaction/2300028

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 18374282HCID 18374282—
SolventDichloromethaneHCID 6344—
ProductHCID 18374274HCID 18374274—

Reaction Steps

Under an atmosphere of nitrogen and with stirring and cooling, a solution of 2.5 g of m-chloroperbenzoic acid in 40 ml of methylene chloride is added dropwise at a temperature of −20° C. to a solution of 2.8 g of ethyl 6-ethylthio-2-trifluoromethylpyridin-3-ylcarboxylate, which had been charged initially, and the mixture is stirred at a temperature of +5° C. for 20 hours. The mixture is then evaporated gently and purified over silica gel (hexanelethyl acetate 7:3). This gives 2.48 g (84%) of 6-ethylsulfinyl-2-trifluoromethylpyridin-3-yl-ethyl ester. 1H NMR (CDCl3, ppm): 8.38 (d, 1H); 8.30 (d, 1H); 4.45 (q, 2H); 3.26-3.00 (m, 2H); 1.43 (t, 3H); 1.26 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498125B2
Source datasetuspto-grants-2002_12
ORD IDord-9a361a32817c4813897686b8a9854fc7
Source noteuspto-grants-2002_12