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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367909Generated: October 31, 2026

1-Ethynyl-4-methoxybenzene → ({4-[(4-Methoxyphenyl)ethynyl]phenyl}ethynyl)(trimethyl)silane

https://huagongshe.com/reaction/2367909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethynyl-4-methoxybenzeneHCID 251020—
Reactant(4-Iodophenylethynyl)trimethylsilaneHCID 11808725—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product({4-[(4-Methoxyphenyl)ethynyl]phenyl}ethynyl)(trimethyl)silaneHCID 1184365098.7%

Reaction Steps

Into a 50 ml round bottom flask was placed a mixture of 0.72 g (0.0054 mole) of p-methoxyphenylacetylene, 1.51 g (0.005 mole) of 4-iodophenyltrimethylsilylacetylene, 0.0102 g (0.0053 mmole) of CuI, 0.102 g (0.146 mmole) of bis(triphenylphosphine)palladium(II)dichloride in 10 ml of THF and 10 ml of triethylamine. The light orange brown mixture was stirred at room temperature under nitrogen for 3 days. The reaction mixture was then filtered and the filtrate concentrated under reduced pressure. The residue was redissolved in 10 ml of chloroform and the solution was washed two times with water (10 ml each) and then dried over anhydrous MgSO4, filtered and concentrated. 1.5 g (98.7% yield) of solid was obtained. 1HNMR: 0.28 ppm (s, 9H); 3.85 ppm (s, 3H); 6.90 ppm (d, 2H); 7.45 ppm (s, 4H); 7.48 ppm (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703388B2
Source datasetuspto-grants-2014_04
ORD IDord-4336af7028874806878b528640384cdb
Source noteuspto-grants-2014_04