Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910102Generated: October 30, 2026

Nitrogen → 1-bromo-4-(phenylethynyl)benzene

https://huagongshe.com/reaction/1910102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPhenylacetyleneHCID 10821—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product1-bromo-4-(phenylethynyl)benzeneHCID 29088899.2%

Reaction Steps

1-Bromo-4-iodobenzene (20.0 g, 70.7 mmol), bis(triphenylphospine)palladium(II) dichloride (PdCl2(PPh3)2) (250 mg), and CuI (68 mg) were suspended in 50 mL triethylamine (NEt3) and 100 mL tetrahydrofuran (THF). The suspension was treated with 3 cycles of evacuation and refilling with N2. Phenylacetylene (7.21 g, 7.75 mL, 1.0 eq) was added in 0.5 mL portions every 5 minutes to the stirred suspension. The solution was then stirred at room temperature for 22 hours. The solvents were then evaporated. Methylene chloride (100 mL) and 1 M HCl (aqueous) (50 mL) were added, the organic layer was retained, and then was washed again with 1 M HCl (aqueous) (50 mL) and 2×50 mL water, dried (MgSO4), filtered, and the solvent evaporated in vacuum to give 18 g of the title compound as a yellow solid, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08599673B2
Source datasetuspto-grants-2013_12
ORD IDord-7bc49786ba7d4c66903f0e1fb8f86fad
Source noteuspto-grants-2013_12