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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259162Generated: October 26, 2026

Triethylamine → 3-Chloro-5-((4-propoxyphenyl)ethynyl)picolinonitrile

https://huagongshe.com/reaction/1259162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dichloro-2-cyanopyridineHCID 2769699—
Reactant1-Ethynyl-4-propoxybenzeneHCID 2775123—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventAmmonium HydroxideHCID 14923—
Product3-Chloro-5-((4-propoxyphenyl)ethynyl)picolinonitrileHCID 66874908—

Reaction Steps

A solution of 3,5-dichloropicolinonitrile (1.0 eq.), 1-ethynyl-4-propoxybenzene (commercially available) (1.0 eq.), trans-dichlororbis(triphenylphosphine)palladium (II) (10 mol %), copper (I) iodide (20 mol %), and triethylamine (5.0 eq.) in DMF (0.3 M) was stirred at 50° C. for 3 hours. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate and 10% aqueous ammonium hydroxide. 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 vaccuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-10% ethyl acetate in hexane to give 3-chloro-5-((4-propoxyphenyl)ethynyl)picolinonitrile as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-54271c7ac05547a4ad45cb3918718d31
Source noteuspto-grants-2013_06