Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116708Generated: October 27, 2026

4-Bromophenol → Phenol, 4-(3-pyridinyl)-

https://huagongshe.com/reaction/2116708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantSodium CarbonateHCID 10340—
Reactant3-Pyridinylboronic acidHCID 2734378—
CatalystHCID 178418397HCID 178418397—
ProductPhenol, 4-(3-pyridinyl)-HCID 15304032.1%

Reaction Steps

Tetrakis(triphenylphosphine)palladium (139 mg, 0.12 mmol) was added to a flask containing 4-bromophenol (519 mg, 3.0 mmol), 3-pyridyl boronic acid (553 mg, 4.5 mmol) and sodium carbonate (1.27 g 12.0 mmol). The flask was flushed with nitrogen and ethanol (6 mL) and water (0.6 mL), were added. The mixture was placed in an oil bath at 80° C. for 16 h. Upon cooling to RT the mixture was partitioned between water and chloroform. The aqueous layer was extracted with chloroform (3×) and the combined organic layers were dried (Na2SO4), filtered and concentrated. The crude residue was purified by chromatography (Biotage, 40S) eluting with 50% ethyl acetate in hexanes to afford 165 mg (32%) of 4-pyridin-3-yl-phenol as a white solid: mp=194.6° C., MS (Cl) m/z 172.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439236B2
Source datasetuspto-grants-2008_10
ORD IDord-5e736cbea095429b81c0235d2cd29fc2
Source noteuspto-grants-2008_10