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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199382Generated: November 1, 2026

m-Chloroperbenzoic acid → 4-Methyl-5-methylsulfinyl-3-(4-pyridyl)-4H-1,2,4-triazole

https://huagongshe.com/reaction/1199382

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-(4-Methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl)pyridineHCID 865987—
SolventDichloromethaneHCID 6344—
Product4-Methyl-5-methylsulfinyl-3-(4-pyridyl)-4H-1,2,4-triazoleHCID 22151475—

Reaction Steps

To a stirred, 0° C., solution of 4-methyl-5-methylthio-3-(4-pyridyl)-4H-1,2,4-triazole (4.54 g, 2.2×10-2 mole) and CH2Cl2 (125 ml) was added portionwise m-chloroperoxybenzoic acid (4.83 g, 2.24×10-2 mole, 80% active MCPBA). After stirring overnight the reaction was diluted with CH2Cl2 until homogeneous. The CH2Cl2 solution was then washed with saturated aqueous NaHCO3 and saturated aqueous NaCl. After drying over anhydrouse Na2SO4, the CH2Cl2 was evaporated at reduced pressure to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04900743
Source datasetuspto-grants-1990_02
ORD IDord-c52e6f478925424aa6a7c7a858abebda
Source noteuspto-grants-1990_02