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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649635Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 178477615, compound

https://huagongshe.com/reaction/1649635

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 178477312HCID 178477312—
SolventDichloromethaneHCID 6344—
ProductHCID 178477615HCID 17847761557%

Reaction Steps

5 g (0.0155 mol) of 1-(4-chlorophenyl)-1-[1-(ethylthio)-1-cyclopropyl]-2-(1,2,4-triazol-yl)-1-ethanol (see Example 1) are stirred with 3.3 g of m-chloroperbenzoic acid (80-90% strength) in 40 ml of methylene chloride overnight at room temperature and then for one hour under reflux. Thereafter, the mixture is washed with twice 20 ml of 5% strength aqueous sodium hydroxide solution and twice with water. The organic phase is dried over sodium sulphate and evaporated down in vacuo. The residue is recrystallized from glycol monomethyl ether acetate. 3 g (57% of theory) of 1-(4-chlorophenyl)-1-[1-(ethylsulphinyl)-1-cyclopropyl]-2-(1,2,4-triazol-yl)1-ethanol of boiling point 185° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921528
Source datasetuspto-grants-1990_05
ORD IDord-47f9012d4fc0422f8a763ba742aaf9aa
Source noteuspto-grants-1990_05