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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199381Generated: November 1, 2026

m-Chloroperbenzoic acid → 3-(2-Fluorophenyl)-5-(methanesulfinyl)-4-methyl-4H-1,2,4-triazole

https://huagongshe.com/reaction/1199381

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-(2-Fluorophenyl)-4-methyl-5-(methylsulfanyl)-4H-1,2,4-triazoleHCID 3087998—
SolventDichloromethaneHCID 6344—
Product3-(2-Fluorophenyl)-5-(methanesulfinyl)-4-methyl-4H-1,2,4-triazoleHCID 3088000—

Reaction Steps

To a stirred, 0° C., solution of 3-(2-fluorophenyl)-4-methyl-5-methylthio-4H-1,2,4-triazole (5.0 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 at room temperature, the reaction was diluted with CH2Cl2 until homogeneous and was then washed in turn twice with saturated aqueous NaHCO3 and once with saturated aqueous NaCl. After drying over anhydrous Na2SO4, the CH2Cl2 was evaporated leaving an oil which slowly crystallized. Crystallization from EtOAc/hexane gave a colorless solid: 3.7 g (68%), mp 95°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04900743
Source datasetuspto-grants-1990_02
ORD IDord-65160f6939574b2eb9f7239b5ad24beb
Source noteuspto-grants-1990_02