HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081735Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 23362947, compound
https://huagongshe.com/reaction/1081735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-[3-(Acetyloxy)propylthio]imidazo[1,2-a]pyridine | HCID 23362878 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23362947 | HCID 23362947 | 34.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05587383 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-af0ba763a3f1404da5163bbb32adfffc |
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| Source note | uspto-grants-1996_12 |
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