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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340229Generated: October 26, 2026

Sodium Carbonate → (E)-3-chloro-5-styrylpicolinonitrile

https://huagongshe.com/reaction/340229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3,5-Dichloro-2-cyanopyridineHCID 2769699—
Reactant4,4,5,5-tetramethyl-2-((E)-2-phenylethenyl)-1,3,2-dioxaborolaneHCID 5708413—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventToluene ethanolHCID 21863594—
Product(E)-3-chloro-5-styrylpicolinonitrileHCID 66875239—

Reaction Steps

A solution of 3,5-dichloropicolinonitrile (1.0 eq.), (E)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane (1.0 eq.), tetrakis(triphenyl-phosphine)palladium (5 mol %), and 2N aqueous sodium carbonate solution (3.4 eq.) in toluene/ethanol (2:1, 0.04 M) was stiffed at 100° C. for 2 hours, then 80° C. for 4 hours. After cooling to ambient temperature, the reaction content was diluted with ethyl acetate and water. The two phases were separated, and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-51af74b6179f4112bbb0aa45874dd4a4
Source noteuspto-grants-2014_11