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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627Generated: October 25, 2026

Sodium Chloride → 4-[(5-Nitro-thien-2-yl)ethynyl]benzonitrile

https://huagongshe.com/reaction/1627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-nitrothiopheneHCID 83222—
Reactant4-EthynylbenzonitrileHCID 4547245—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[(5-Nitro-thien-2-yl)ethynyl]benzonitrileHCID 19691953—

Reaction Steps

To a solution of 4-ethynylbenzonitrile (0.5 g), 2-bromo-5-nitrothiophene (0.9 g) and bis(triphenylphosphine)palladium dichloride (83 mg) in anhydrous dimethylformamide (4 ml) was added triethylamine (2.2 ml). The reaction mixture was stirred at room temperature for 3 days then ethyl acetate (200 ml) and saturated sodium chloride (200 ml) were added. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to dryness. The crude solid was triturated with 1:1 dichloromethane/hexane followed by diethyl ether to give 4-[(5-nitro-2-thienyl)ethynyl]benzonitrile as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726195
Source datasetuspto-grants-1998_03
ORD IDord-f537d62089cd4cba9bc833054c2f705b
Source noteuspto-grants-1998_03