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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254063Generated: November 1, 2026

Bromine → 2-bromo-1-(6-bromopyridin-3-yl)ethanone

https://huagongshe.com/reaction/1254063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Acetyl-2-bromopyridineHCID 15668195—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2-bromo-1-(6-bromopyridin-3-yl)ethanoneHCID 10850267—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(6-Bromopyridin-3-yl)ethanone was dissolved in 50 mL of chloroform and cooled to 0° C., to which was added catalytic amount of AlCl3 and 2.65 mL of bromine in 25 mL of chloroform. The addition of bromine lasted 1 h to keep the reaction solution at 0° C. After stirring at 0° C. overnight, the mixture was diluted with dichloromethane, washed with aqueous sodium bicarbonate, water, and brine. The organic layer was dried (MgSO4), filtered, and concentrated to afford 2-bromo-1-(6-bromopyridin-3-yl)ethanone which was used in the next step with out further purification. LCMS: [M+1]+=279.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455528B2
Source datasetuspto-grants-2013_06
ORD IDord-4940eecbd9234b88a4be7fbf6fac94c9
Source noteuspto-grants-2013_06