Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230978Generated: November 1, 2026

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

https://huagongshe.com/reaction/2230978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
Reactant3-BromopyridineHCID 12286—
ReactantSodium BicarbonateHCID 516892—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product3-(3-Nitrophenyl)pyridineHCID 12181327—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 3-bromopyridine (2.6 ml) and tetrakis(triphenylphosphine)palladium(0) (0.93 g) in toluene (50 ml) was added 2M 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 6 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 (3:7)) to give 3-(3-nitrophenyl)pyridine (3.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-81143af525e444d1bf0add2619778c76
Source noteuspto-grants-2002_07