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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499325Generated: October 31, 2026

Ethyl Acetate → 2-Thien-2-ylisonicotinonitrile

https://huagongshe.com/reaction/499325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-cyanopyridineHCID 568638—
Reactant2-Thienylboric acidHCID 15138998—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent2-Methylphenethyl alcoholHCID 88267—
Product2-Thien-2-ylisonicotinonitrileHCID 5106401652.2%

Reaction Steps

2-Chloro-4-cyanopyridine (0.50 g, 3.6 mmol) and 2-thienylboric acid (0.69 g, 5.4 mmol) were dissolved in toluene-ethanol (4:1, v/v, 25 ml), and to the mixture, a solution of potassium carbonate (1.3 g, 9.0 mmol) in water (5 ml) was added. The mixture was deairated under reduced pressure for 15 minutes. Tetrakis(triphenylphosphine)palladium (0.21 mg, 0.2 mmol) was added to the mixture under nitrogen atmosphere, and the mixture was refluxed for 20 hrs. The reaction mixture was combined with ethyl acetate and water. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to a silica gel (60 g) column chromatography and eluted with hexane-ethyl acetate (3:1, v/v) to give solid, which was recrystallized from ethanol to give the titled compound (0.35 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767665B2
Source datasetuspto-grants-2010_08
ORD IDord-0218e8ad33104ecd8521bf4642f68f22
Source noteuspto-grants-2010_08