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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086801Generated: October 30, 2026

3-Nitrophenylboronic Acid → 2-(3-Nitrophenyl)pyridine

https://huagongshe.com/reaction/2086801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
Reactant2-BromopyridineHCID 7973—
ReactantSodium BicarbonateHCID 516892—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(3-Nitrophenyl)pyridineHCID 459555—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-bromopyridine (1.91 ml) and tetrakis(triphenylphosphine)palladium(0) (0.46 g) in 1,2-dimethoxyethane (40 ml) was added 2M aqueous solution of sodium bicarbonate (20 ml) and a solution of dihydroxy(3-nitrophenyl)borane (3.67 g) in methanol (10 ml). The mixture was stirred at 80° C. for 2.5 hours 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 (hexane-ethyl acetate (3:1)) to give 2-(3-nitrophenyl)pyridine (1.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727245B2
Source datasetuspto-grants-2004_04
ORD IDord-a21882dac61041a7bf8131fc2b37317e
Source noteuspto-grants-2004_04