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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467116Generated: October 30, 2026

m-Chloroperbenzoic acid → 3-(Methanesulfinyl)-4-methyl-5-(naphthalen-2-yl)-4H-1,2,4-triazole

https://huagongshe.com/reaction/467116

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4H-1,2,4-Triazole, 4-methyl-3-(methylthio)-5-(2-naphthalenyl)-HCID 3087999—
SolventDichloromethaneHCID 6344—
Product3-(Methanesulfinyl)-4-methyl-5-(naphthalen-2-yl)-4H-1,2,4-triazoleHCID 3088002—

Reaction Steps

To a stirred, 0° C., solution of 4-methyl-5-methylthio-3-(2-naphthyl)-4H-1,2,4-triazole (4.00 g, 1.57×10-2 mole) and CH2Cl2 (110 ml) was added portionwise m-chloroperoxybenzoic acid (3.38 g, 1.57×10-2 mole). After stirring overnight at room temperature the reaction was diluted with CH2Cl2 (200 ml), washed two times with saturated aqueous NaHCO3 and one time with saturated aqueous NaCl, and dried over anhydrous Na2SO4. The drying agent was removed by filtration and the filtrate was evaporated at reduced pressure leaving an off-white solid which was purified by flash chromatography (4% CH3OH/CH2Cl2). Crystallization from toluene afforded small colorless plates: Mp 224°-226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158968
Source datasetuspto-grants-1992_10
ORD IDord-ca2875cfa6fc4d0eb438fadbe037d7ba
Source noteuspto-grants-1992_10