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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230960Generated: November 1, 2026

3-Bromopyridine → 3-[(E)-2-(3-nitrophenyl)vinyl]pyridine

https://huagongshe.com/reaction/2230960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant3-NitrostyreneHCID 68514—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product3-[(E)-2-(3-nitrophenyl)vinyl]pyridineHCID 22724484—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 3-nitrostyrene (4.6 ml), 3-bromopyridine (2.6 ml), palladium(II) acetate (0.20 g), tetrabutylammonium chloride (8.4 g) and sodium bicarbonate (6.3 g) in N,N-dimethylformamide (40 ml) was stirred at 110° C. for 3 hours. 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 resultant solid was collected and washed with isoprbpyl ether to give 3-[(E)-2-(3-nitrophenyl)vinyl]pyridine (5.34 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-38072d3196fe4c058788c8ee20f28646
Source noteuspto-grants-2002_07