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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594419Generated: October 30, 2026

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

https://huagongshe.com/reaction/1594419

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BisulfiteHCID 23665763—
Reactant3-Methylthio-5-(cyclohexyl)methyl-1,2,4-thiadiazoleHCID 58610439—
SolventChloroformHCID 6212—
Product3-Methylsulfonyl-5-(cyclohexyl)methyl-1,2,4-thiadiazoleHCID 69024542—

Reaction Steps

1.2 g of 3-methylthio-5-(cyclohexyl)methyl-1,2,4-thiadiazole was dissolved in 20 ml of chloroform, 2.78 g of 3-chloroperoxybenzoic acid (content>65%) was added thereto, and the reaction mixture was stirred for 1 hour under ice-cooling and for 16 hours at 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 1.4 g of 3-methylsulfonyl-5-(cyclohexyl)methyl-1,2,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07301032B2
Source datasetuspto-grants-2007_11
ORD IDord-59a78a59556248c28fc5abf310fb4ea5
Source noteuspto-grants-2007_11