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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895892Generated: October 30, 2026

Benzyl Bromide → 1-Benzyl-3-bromo-5-chloro-2-pyridone

https://huagongshe.com/reaction/895892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-5-chloropyridin-2-olHCID 2726791—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventEthyl AcetateHCID 8857—
Product1-Benzyl-3-bromo-5-chloro-2-pyridoneHCID 2238205431.1%

Reaction Steps

A mixture of 3-bromo-5-chloro-1H-2-pyridone (950 mg, 4.56 mmol), freshly ground potassium carbonate (1.26 g, 9.1 mmol) and tetrabutyl ammonium chloride (100 mg) in was stirred mechanically without solvent for 30 min and benzyl bromide (0.56 mL, 4.7 mmol) was added. The mixture was stirred at room temperature for 72 hr. The mixture was diluted with ethyl acetate and filtered, washing the solids with ethyl acetate. The filtrate was evaporated to dryness and the residue was triturated with several portions of hexane. The residue was chromatographed over 90 g of silica gel eluting with 3:1 hexane:ethyl acetate followed by 100% ethyl acetate to give 1-benzyl-3-bromo-5-chloro-2-pyridone (423 mg, 31%), mp 108-110° C. LR(+)LSIMS: m/z 595 (2M+H, 2 Cl, 2 Br), 298 (M+H, 1 Cl, 1 Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916933B2
Source datasetuspto-grants-2005_07
ORD IDord-18ca42917f424cbcbece01bd7afc719b
Source noteuspto-grants-2005_07