HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644141Generated: October 31, 2026
1-Ethynyl-4-methoxybenzene → ({4-[(4-Methoxyphenyl)ethynyl]phenyl}ethynyl)(trimethyl)silane
https://huagongshe.com/reaction/1644141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Ethynyl-4-methoxybenzene | HCID 251020 | — |
| Reactant | (4-Iodophenylethynyl)trimethylsilane | HCID 11808725 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | ({4-[(4-Methoxyphenyl)ethynyl]phenyl}ethynyl)(trimethyl)silane | HCID 11843650 | 98.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124299B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-33767b9b2c4e4c73a5df2d73d602bea6 |
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| Source note | uspto-grants-2012_02 |
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