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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885278Generated: November 2, 2026

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

https://huagongshe.com/reaction/1885278

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 numberUS05143933
Source datasetuspto-grants-1992_09
ORD IDord-d1abe9afc9514736b23b52ec051a6a20
Source noteuspto-grants-1992_09