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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230976Generated: October 30, 2026

3-Nitrophenylboronic Acid → 4-(3-Nitrophenyl)pyridine

https://huagongshe.com/reaction/2230976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
Reactant4-Bromopyridinium chlorideHCID 88100—
ReactantSodium BicarbonateHCID 516892—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product4-(3-Nitrophenyl)pyridineHCID 45955764%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 4-bromopyridine hydrochloride (5.25 g) and tetrakis(triphenylphosphine)palladium(0) (0.93 g) in toluene (50 ml) was added 3M aqueous solution of sodium bicarbonate (27 ml) and a solution of dihydroxy(3-nitrophenyl)borane (5.0 g) in methanol (12 ml). The mixture was stirred at 80° C. for 1 hour and cooled. Then the mixture was poured into aqueous sodium bicarbonate and extracted with ethyl acetate twice. The combined organic phase was washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel (1%-2% methanol in chloroform) to give 4-(3-nitrophenyl)pyridine (3.46 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-88e5cc112c8e4e0f9a9f3db30aeee6e8
Source noteuspto-grants-2002_07