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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626Generated: October 25, 2026

Triethylamine → 4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrile

https://huagongshe.com/reaction/1626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-nitrofuranHCID 233582—
Reactant4-EthynylbenzonitrileHCID 4547245—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrileHCID 19691951—

Reaction Steps

To a solution of 2-bromo-5-nitrofuran (1.65 g) and triethylamine (34 ml) in anhydrous acetonitrile (55 ml) under nitrogen was added bis(triphenylphosphine)palladium dichloride (130 mg) and cuprous iodide (35 mg). 4-Ethynylbenzonitrile (1.09 g) was added and the reaction mixture was stirred under nitrogen overnight. The mixture was evaporated to dryness and the residue was dissolved in dichloromethane (200 ml), dried over anhydrous sodium sulfate, filtered and evaporated to dryness. The residue was purified by silica gel chromatography (ethyl acetate/hexane 1:10) and triturated with ethyl acetate/hexane (1:3) to give 4-[(5-nitro-2-furyl)-ethynyl]benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726195
Source datasetuspto-grants-1998_03
ORD IDord-fd2ce529eb5e4230a968d9b7a9207cfc
Source noteuspto-grants-1998_03