HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493030Erstellt: 25. Oktober 2026
Hydrochloric Acid → 1-(4-n-Propylphenyl)-2-trimethylsilylacetylene
https://huagongshe.com/reaction/493030
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | 1-Bromo-4-propylbenzene | HCID 136374 | — |
| Katalysator | Triphenylphosphine | HCID 11776 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(4-n-Propylphenyl)-2-trimethylsilylacetylene | HCID 19353401 | 87,1% |
Reaktionsschritte
To 15.0 g (75.4 mmol) of 1-n-propyl-4-bromobenzene were added 8.8 g (89.8 mmol) of trimethylsilylacetylene and 100 ml of triethylamine (NEt3), and the reaction system was purged with argon. Next were added 81 mg (0.4 mmol) of copper (I) iodide (CuI), 324 mg (1.2 mmol) of triphenylphosphine, and 162 mg of dichlorobistriphenylphosphine palladium (II) [PdCl2(PPh3)2] to the reaction system, and the mixture was subjected to reaction for 24 hours with heating and refluxing. After completion of the reaction, the reaction mixture was poured into an iced water, and the resultant mixture was acidified by adding hydrochloric acid. After the resultant water-insoluble oil was extracted with hexane, the hexane phase was washed with water. By removing hexane from the hexane phase, 14.2 g (65.7 mmol) of 1-(4-n-propylphenyl)-2-trimethylsilylacetylene was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07534547B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-41c7fd2116914f8b8f5c9d25ee7d1452 |
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| Quellennotiz | uspto-grants-2009_05 |
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