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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230977Generated: October 31, 2026

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

https://huagongshe.com/reaction/2230977

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 numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-b22717275bb94179a03dbc61dca0fa4a
Source noteuspto-grants-2002_07