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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090324Generated: November 3, 2026

Ethanol → HCID 178527214, compound

https://huagongshe.com/reaction/1090324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178420288HCID 178420288—
SolventChloroformHCID 6212—
ProductHCID 178527214HCID 178527214—

Reaction Steps

2-[(2-Phenylethyl)thio]-1H-imidazo[4,5-c]pyridine (2.4 g, 0.0094 mol) was dissolved in 120 mL of chloroform with heating. The reaction solution was cooled in an ice bath to 0°-5° C. m-Chloroperoxybenzoic acid (1.91 g, 0.0094 mol) was added portionwise. The reaction mixture was then stirred at room temperature for 1 hour. 10% aqueous sodium bicarbonate was added and the organic layer was separated and dried over magnesium sulfate. After filtering, the filtrate was evaporated to half the volume in a rotary evaporator. Ether was added to the cloudy point and the reaction mixture was cooled in ice. The crystals that had formed amounted to 0.63 g. An analytical sample, m.p. 171°-174° C., was obtained by recrystallization from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081253
Source datasetuspto-grants-1992_01
ORD IDord-49bd0b81e46a43c1808c311bdd0040f2
Source noteuspto-grants-1992_01