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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584735Generated: October 30, 2026

m-Chloroperbenzoic acid → 1,5-bis(4-methoxyphenyl)-3-(methylsulfonyl)-1H-1,2,4-triazole

https://huagongshe.com/reaction/584735

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant1,5-bis(4-methoxyphenyl)-3-(methylsulfinyl)-1H-1,2,4-triazoleHCID 10268992—
SolventDichloromethaneHCID 6344—
Product1,5-bis(4-methoxyphenyl)-3-(methylsulfonyl)-1H-1,2,4-triazoleHCID 996878881.7%

Reaction Steps

A mixture of 1,5-bis(4-methoxyphenyl)-3-(methylsulfinyl)-1H-1,2,4-triazole (152 mg, 0.443 mmol) and m-chloroperbenzoic acid (115 mg, 0.664 mmol) in dichloromethane (1.5 mL) was stirred at room temperature for 6 hours. Dichloromethane and sat. sodium bicarbonate solution were poured into the mixture and the organic layer was separated. The aqueous layer was extracted with dichloromethane. A combined organic layer was washed with sat. sodium bicarbonate solution and brine and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was triturated with diisopropyl ether and the precipitate was isolated by filtration, washed with diisopropyl ether, and dried in vacuo to give 1,5-bis(4-methoxyphenyl)-3-(methylsulfonyl)-1H-1,2,4-triazole (130 mg, 81.7% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927230B2
Source datasetuspto-grants-2005_08
ORD IDord-14d159d1008045edbab71a28d3c1cd2b
Source noteuspto-grants-2005_08