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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571047Generated: October 31, 2026

N-Bromosuccinamide → 3-(benzyloxy)-5-bromo-1-(4-butylphenyl)pyridin-4(1H)-one

https://huagongshe.com/reaction/571047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BromosuccinamideHCID 9834204—
Reactant3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-oneHCID 67419599—
SolventAcetic AcidHCID 176—
Product3-(benzyloxy)-5-bromo-1-(4-butylphenyl)pyridin-4(1H)-oneHCID 67419034—

Reaction Steps

To a solution of 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one (705 mg, 2.1 mmol) in AcOH (21 mL) was added N-bromosuccinamide (414 mg, 2.3 mmol) and the reaction mixture was stirred at room temperature. After 1 h, the mixture was concentrated under reduced pressure and purified by flash chromatography (50 g SiO2, 0-70% ethyl acetate/hexanes) to provide 3-(benzyloxy)-5-bromo-1-(4-butylphenyl)pyridin-4(1H)-one. LC/MS (M+H)+ 412/414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024032B2
Source datasetuspto-grants-2015_05
ORD IDord-bdc6f27d6a104e5d92a7e98d0c899522
Source noteuspto-grants-2015_05