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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864494Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 68592779, compound

https://huagongshe.com/reaction/1864494

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 59710226HCID 59710226—
SolventChloroformHCID 6212—
ProductHCID 68592779HCID 685927798.5%

Reaction Steps

Cis-3,5-Dimethyl-4-(3-oxo-butyl)-piperazine-1-carboxylic acid tert-butyl ester (1.00 g) in chloroform (40 mL) was treated with m-chloroperbenzoic acid (77%, 0.97 g ) at 0° C. The solution was allowed to warm to room temperature and stirred overnight. The reaction mixture was then cooled to 0° C., filtered to remove precipitates, washed with saturated aqueous sodium bicarbonate, filtered through a plug of silica gel and concentrated. The residue was taken up in a 1:1 mixture of DCM and MeOH and treated with an excess of 4.0 M HCl/dioxane. The reaction mixture was stirred overnight and then purified by column chromatography (0 to 10% MeOH:DCM) to yield 50 mg of the title compound. ESMS (0.41 minutes, (M+1) 131.13, Method E).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625909B2
Source datasetuspto-grants-2009_12
ORD IDord-63c0a4b3f56e48f2bd91d217da33c254
Source noteuspto-grants-2009_12