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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479508Generated: October 26, 2026

m-Chloroperbenzoic acid → 3-(benzyloxy)-5-bromopyridine N-oxide

https://huagongshe.com/reaction/1479508

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-(Benzyloxy)-5-bromopyridineHCID 15389198—
SolventDichloromethaneHCID 6344—
Product3-(benzyloxy)-5-bromopyridine N-oxideHCID 58213489—

Reaction Steps

A solution of 3-(benzyloxy)-5-bromopyridine (from step 1) (1.0 eq.) and meta-chloroperbenzoic acid (mCPBA) (4.0 eq.) in dichloromethane (0.1 M) was stirred at room temperature for 18 hours. The reaction was quenched with saturated aqueous NaHCO3 solution and extracted with dichloromethane three times. The combined organic layers were dried over anhydrous MgSO4 and concentrated en vacuo. The crude residue was purified by a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane to give 3-(benzyloxy)-5-bromopyridine 1-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-61589c04e9bc4a52aa1ea0921ecefa4c
Source noteuspto-grants-2016_08