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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256182Generated: October 27, 2026

m-Chloroperbenzoic acid → HCID 57815209, compound

https://huagongshe.com/reaction/1256182

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Bromo-1,5-naphthyridineHCID 12878818—
SolventDichloromethaneHCID 6344—
ProductHCID 57815209HCID 57815209—
ProductHCID 58310524HCID 58310524—

Reaction Steps

4.43 g (21.2 mmol, 1 eq) of 3-bromo-1,5-naphthyridine (W. Czuba, Recueil des Travaux Chimiques des Pays-Bas 1963, 82, 988-996) were introduced in 165 mL of methylene chloride. 5.23 g (21.2 mmol, 1 eq) of meta-chloroperbenzoic acid were then added portionwise at 0° C. The mixture was stirred at rt for 18 h. The mixture was washed with 1M aqueous NaOH solution and water. Organic layer was dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by column chromatography using methylene chloride and then methylene chloride/ethanol: 98/2 as eluent. The solvent was evaporated to dryness to afford 3.08 g of 3-bromo-1,5-naphthyridine-5-oxide (pale yellow powder) with 64% yield and 1.00 g of 3-bromo-1,5-naphthyridine-1-oxide (yellow powder) with 21% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461178B2
Source datasetuspto-grants-2013_06
ORD IDord-157d1c9e7e6e45b4b3e95202712b7e8c
Source noteuspto-grants-2013_06