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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606838Generated: October 25, 2026

Triethylamine → 5-(3,4-Dimethylphenylethynyl)-nicotinonitrile

https://huagongshe.com/reaction/606838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Iodo-1,2-dimethylbenzeneHCID 141646—
Reactant5-EthynylnicotinonitrileHCID 22416563—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178419050HCID 178419050—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product5-(3,4-Dimethylphenylethynyl)-nicotinonitrileHCID 6704754262%

Reaction Steps

Combine 4-iodo-o-xylene (0.362 g, 1.561 mmol), bis(triphenylphosphine)palladium (II) dichloride (55 mg, 0.078 mmol), and copper (I) iodide (30 mg, 0.156 mmol) in triethylamine (0.653 mL, 4.683 mmol) and stir under nitrogen for 5 min at 80° C. Add a solution of 5-ethynylnicotinonitrile, (prepared essentially as described in PREPARATION 4), (200 mg, 1.561 mmol) in anhydrous acetonitrile (2.50 mL), and stir under nitrogen overnight. Cool to room temperature and dilute with diethyl ether. Wash with a saturated aqueous solution of sodium bicarbonate, dry (sodium sulfate), filter, and concentrate. Purify the residue by silica gel chromatography, eluting with 95:5 to 50:50 dichloromethane:ethyl acetate, to give the title compound as a yellow solid (225 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-f070616815b445c8816ea82e3b9c3f6a
Source noteuspto-grants-2011_03