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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090323Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 178527207, compound

https://huagongshe.com/reaction/1090323

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 178420433HCID 178420433—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 178527207HCID 178527207—

Reaction Steps

To a chilled (0°-5° C.) solution of 3.3 g (0.014 mol) of 2-[[(phenyl)methyl]thio]-1H-imidazo[4,5-c]pyridine in 50 mL of chloroform and 5 mL of methanol was added dropwise a solution containing 2.78 g (0.014 mol) of m- chloroperoxybenzoic acid in 50 mL of chloroform. The reaction mixture was then stirred at room temperture for 45 minutes. Approximately one half of the chloroform was removed in a rotary evaporator and the reaction mixture was then poured into 200 mL of ether. The reaction mixture was cooled in ice. The precipitate that formed was collected and amounted to 1.78 g. The product was suspended in aqueous 10% sodium bicarbonate solution, filtered and was air dried overnight. The product amounted to 1.39 g. An analytical sample (m.p. 190°-193° C.) was obtained by recrystallization from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081253
Source datasetuspto-grants-1992_01
ORD IDord-53dfd3426b544100bd425c6728cae632
Source noteuspto-grants-1992_01