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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875421Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 86720634, compound

https://huagongshe.com/reaction/875421

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86720633HCID 86720633—
SolventDichloromethaneHCID 6344—
ProductHCID 86720634HCID 8672063499%

Reaction Steps

A stirred suspension of benzyl 3-chloro-1H-pyrrolo[3,2-c]pyridine-1-carboxylate (2.4 g, 8.37 mmol) in dichloromethane (20 mL) was treated portion wise with 3-chloroperoxybenzoic acid (2.165 g, 12.55 mmol) followed by stirring at room temperature for about 1.5 hours. The reaction was neutralized with saturated aq. sodium bicarbonate solution. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated to afford benzyl 3-chloro-1H-pyrrolo[3,2-c]pyridine-1-carboxylate 5-oxide (2.45 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980911B2
Source datasetuspto-grants-2015_03
ORD IDord-ab87b60cec674e368d2a64c88062eaba
Source noteuspto-grants-2015_03