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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594424Generated: October 26, 2026

m-Chloroperbenzoic acid → 3-Methylsulfonyl-5-(2-methylcyclohexyl)-1,2,4-thiadiazole

https://huagongshe.com/reaction/1594424

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BisulfiteHCID 23665763—
Reactant5-(2-Methylcyclohexyl)-3-methylthio-1,2,4-thiadiazoleHCID 58610442—
SolventChloroformHCID 6212—
Product3-Methylsulfonyl-5-(2-methylcyclohexyl)-1,2,4-thiadiazoleHCID 69027281—

Reaction Steps

500 mg of 5-(2-methylcyclohexyl)-3-methylthio-1,2,4-thiadiazole was dissolved in 6.5 ml of chloroform, 1.62 g of 3-chloroperoxybenzoic acid (content>65%) was added thereto taking for 20 minutes, and the reaction mixture was stirred for 30 minutes under ice-cooling and for 1.5 hours under room temperature. Then, the reaction mixture was added to saturated sodium hydrogensulfite aqueous solution, and separated. The organic layer was washed with sodium hydrogencarbonate aqueous solution, dried over anhydrous sodium sulfate, concentrated to give 466 mg of 3-methylsulfonyl-5-(2-methylcyclohexyl)-1,2,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07301032B2
Source datasetuspto-grants-2007_11
ORD IDord-d6bce006443c4f34916cebb22f0cf0b6
Source noteuspto-grants-2007_11