HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59334Erstellt: 23. Oktober 2026
Trimethylsilylacetylene → 1-[(Trimethylsilyl)ethynyl]-3-(trifluoromethyl)benzene
https://huagongshe.com/de/reaction/59334
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | Benzene, 1-iodo-3-(trifluoromethyl)- | HCID 67868 | — |
| Katalysator | Copper iodide | HCID 83717 | — |
| Katalysator | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-[(Trimethylsilyl)ethynyl]-3-(trifluoromethyl)benzene | HCID 4281885 | 57,3% |
Reaktionsschritte
To a solution of 1-iodo-3-(trifluoromethyl)benzene (1.0 g, 3.6 mmol) in ethyl acetate (20 mL) was added ethynyl(trimethyl)silane (0.540 g, 5.5 mmol), copper iodide (0.042 g, 0.22 mmol), bis(triphenylphosphine) palladium(II) chloride (0.129 g, 0.18 mmol) and TEA (2.2 mL, 14.7 mmol). The reaction mass stirred at 50-60° C. for 24 h. The reaction mass was quenched in water, extracted with ethyl acetate and concentrated to afford 0.500 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 0.26 (s, 9H), 7.44 (t, J=7.8 Hz, 1H), 7.55 (d, J=7.8 Hz, 1H), 7.62 (d, J=7.2 Hz, 1H), 7.72 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09439890B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-db091dd852e94dac8377a99e56e3cd33 |
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| Quellennotiz | uspto-grants-2016_09 |
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