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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201814Generated: October 29, 2026

m-Chloroperbenzoic acid → HCID 86720634, compound

https://huagongshe.com/reaction/2201814

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 numberUS09364466B2
Source datasetuspto-grants-2016_06
ORD IDord-a82af03e02574339a9a1e0eef32d8a8e
Source noteuspto-grants-2016_06