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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259149Generated: November 1, 2026

Triethylamine → 3-Chloro-5-(p-tolylethynyl)picolinonitrile

https://huagongshe.com/reaction/1259149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantp-EthynyltolueneHCID 13018—
Reactant3,5-Dichloro-2-cyanopyridineHCID 2769699—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventAmmonium HydroxideHCID 14923—
Product3-Chloro-5-(p-tolylethynyl)picolinonitrileHCID 66875734—

Reaction Steps

A solution of 3,5-dichloropicolinonitrile (commercially available) (1.0 eq.), 1-ethynyl-4-methylbenzene (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 stirring in hot ether/hexane mixtures and filtered to give 3-chloro-5-(p-tolylethynyl)picolinonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-cf8666accd1e481e97f01b3b2558821b
Source noteuspto-grants-2013_06