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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271509Generated: October 31, 2026

Potassium Carbonate → 4-(3-Bromo-furan-2-yl)-pyridine

https://huagongshe.com/reaction/271509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant2,3-DibromofuranHCID 7021501—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(3-Bromo-furan-2-yl)-pyridineHCID 1572183154%

Reaction Steps

A degassed mixture of 2,3-dibromofuran (11.3 g, 50 mmol), 4-pyridyl boronic acid (M. Lamothe et al, J. Med. Chem., 1997, 40, 3542) (6.15 g, 50 mmol) and potassium carbonate (55 g, 0.4 mol) in ethylene glycol dimethyl ether (300 ml) and water (150 ml) was treated with triphenylphosphine (1.31 g, 5 mmol) and palladium acetate (625 mg, 2.5 mmol) then heated under reflux for 18 hours. After cooling to room temperature, the mixture was filtered through filter aid and the filtrate diluted with water and ethyl acetate. The organic phase was separated, washed with water and brine, dried, concentrated in vacuo and the residue purified by silica gel chromatography to give the title compound (6.0 g, 54%); MS(ES+) m/e 224/226 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452906B2
Source datasetuspto-grants-2008_11
ORD IDord-5e621bab50a446d88380f65519c7033d
Source noteuspto-grants-2008_11