HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217445Erstellt: 24. Oktober 2026
Hydrochloric Acid → [(4-Isobutylphenyl)ethynyl](trimethyl)silane
https://huagongshe.com/de/reaction/217445
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | 1-Bromo-4-(2-methylpropyl)benzene | HCID 3789018 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | [(4-Isobutylphenyl)ethynyl](trimethyl)silane | HCID 58438693 | 42,5% |
Reaktionsschritte
To a solution of Pd(PPh3)4 (542 mg) and TEA (4 mL) in DMF (16 mL) were added 1-bromo-4-isobutylbenzene (1 g) and ethynyl(trimethyl)silane (553 mg) at room temperature, followed by stirring at 60° C. for 4 hours. To the reaction liquid was added 1 M hydrochloric acid, followed by extraction with ether. The insoluble materials were filtered through celite. The organic layer was washed with brine, dried over MgSO4, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane) to obtain [(4-isobutylphenyl)ethynyl](trimethyl)silane (459 mg) as a yellow liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08193378B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-f1e45472360443ac87ab58d8f3ec8a95 |
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| Quellennotiz | uspto-grants-2012_06 |
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