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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231005Generated: November 1, 2026

3,5-Dichloropyridine → HCID 22724426, compound

https://huagongshe.com/reaction/2231005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DichloropyridineHCID 17153—
Reactant3-NitrostyreneHCID 68514—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 22724426HCID 2272442646.2%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 3-nitrostyrene (3.98 g), 3,5-dichloropyridine (3.70 g), palladium(II) acetate (0.20 g), tetrabutylammonium chloride (7.0 g) and sodium bicarbonate (5.3 g) in N,N-dimethylformamide (35 ml) was stirred at 135° C. for 2 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 isopropyl ether to give 3-chloro-5-[(E)-2-(3-nitrophenyl)vinyl]pyridine (3.01 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-e5610734672744a39625df24de330e2b
Source noteuspto-grants-2002_07