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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227114Generated: October 27, 2026

Sodium Carbonate → 5-Bromo-2-(4-octylphenyl)pyridine

https://huagongshe.com/reaction/2227114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,3-DibromopyridineHCID 817102—
Reactant(4-octylphenyl)boronic AcidHCID 4197992—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product5-Bromo-2-(4-octylphenyl)pyridineHCID 1847182095%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a 1000 mL round bottom flask equipped with a stirbar was added dibromopyridine 7C (22.506 g), boronic acid 7B (22.356 g), tetrakis(triphenylphosphine)palladium(0) (3.294 g), saturated sodium carbonate solution (238 mL), and toluene (190 mL). A reflux condenser was attached and the reaction was heated at 100° C. for 24 hours. The cooled reaction mixture was extracted with 1:1 hexane:ethyl acetate, and the combined organic layers were washed with brine and dried over magnesium sulfate and the solvent was removed in vacuo. The solid product was dissolved in dichloromethane, placed on silica gel, and silica gel filtered. The elution solvents were hexane, which removed a higher Rf side product, and 2.5% E/H, resulting in 31.251 g of solid. The product was recrystallized from acetonitrile to give 30.125 g of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413448B1
Source datasetuspto-grants-2002_07
ORD IDord-084f9497f27543ada529675940335893
Source noteuspto-grants-2002_07