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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035738Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 178451080, compound

https://huagongshe.com/reaction/1035738

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 178451079HCID 178451079—
SolventDichloromethaneHCID 6344—
ProductHCID 178451080HCID 178451080118.2%

Reaction Steps

0.1 g of tert-butyl trans-{4-[4-(5-benzylsulfanylmethyl[1.3.4]thiadiazol-2-ylcarbamoyl)-phenyl]cyclohexyl}acetate (0.11 mmol, 1 eq.) is placed in 10 mL of dichloromethane with stirring. 0.027 g of 70% meta-chloroperbenzoic acid (0.11 mmol, 1 eq.) is added. After 2 hours, 0.01 g of 70% meta-chloroperbenzoic acid (0.41 mmol, 0.37 eq.) is added. After 16 hours, the reaction medium is diluted with dichloromethane and washed with saturated aqueous sodium hydrogen carbonate solution. The organic phase is dried and evaporated. The residue is triturated in ethyl acetate to give 0.072 g of tert-butyl trans-{4-[4-(5-phenylmethanesulfinylmethyl[1.3.4]thiadiazol-2-ylcarbamoyl)-phenyl]cyclohexyl}acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546391B2
Source datasetuspto-grants-2013_10
ORD IDord-6fe10f64826a41268c76ad771b528bc9
Source noteuspto-grants-2013_10