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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086802Generated: October 30, 2026

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

https://huagongshe.com/reaction/2086802

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 numberUS06727245B2
Source datasetuspto-grants-2004_04
ORD IDord-9272dc126c7b4ee286d27f2520950303
Source noteuspto-grants-2004_04