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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199383Generated: November 4, 2026

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

https://huagongshe.com/reaction/1199383

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4H-1,2,4-Triazole, 4-methyl-3-(methylthio)-5-(2-thienyl)-HCID 611089—
SolventDichloromethaneHCID 6344—
Product3-(Methanesulfinyl)-4-methyl-5-(thiophen-2-yl)-4H-1,2,4-triazoleHCID 3088001—

Reaction Steps

To a stirred, 0° C., solution of 4-methyl-5-methylthio-3-(2-thienyl)-4H-1,2,4-triazole (4.85 g, 2.29×10-2 mole) and CH2Cl2 (170 ml) was added portionwise m-chloroperoxybenzoic acid (4.95 g, 2.29×10-2 mole). After stirring at room temperature overnight the reaction was washed two times with saturated aqueous NaHCO3 and one time with saturated aqueous NaCl, and dried over anhydrous N2SO4. The drying agent was removed by filtration and the filtrate was evaporated at reduced pressure yielding an off-white solid which was purified by flash chromatography (40% acetone/EtOAc). Crystallization from EtOAc afforded small colorless plates: 2.78 g (53%), mp 105°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04900743
Source datasetuspto-grants-1990_02
ORD IDord-dc97481fa9ec4fe18d3199dc6192a7d2
Source noteuspto-grants-1990_02