Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081735Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 23362947, compound

https://huagongshe.com/reaction/1081735

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-[3-(Acetyloxy)propylthio]imidazo[1,2-a]pyridineHCID 23362878—
SolventChloroformHCID 6212—
ProductHCID 23362947HCID 2336294734.6%

Reaction Steps

To a solution of 5-[3-(acetyloxy)propylthio]imidazo[1,2-a]pyridine (1.00 g, 3.99 mmoles) in chloroform (25 ml) was added m-chloroperbenzoic acid (1.47 g, 5.96 mmoles) with stirring under ice-cooling and the mixture was further stirred under ice-cooling for 1.5 hours. The reaction mixture was washed in turn with an aqueous 20% sodium bisulfite solution and an aqueous saturated sodium bicarbonate solution and dried. After the solvent was distilled off, the residue was purified by column chromatography [eluent:hexane/acetone (1:1)] to obtain 0.19 g of 5-[3-(acetyloxy)propylsulfinyl]imidazo[1,2-a]pyridine (Compound 177) (34.6%, yellow oily product) and 0.19 g of 5-(acetyloxy)propylsulfonyl]imidazo[1,2-a]pyridine (Compound 178) (16.5%, yellow oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-af0ba763a3f1404da5163bbb32adfffc
Source noteuspto-grants-1996_12