Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 1-(Decyloxy)-4-ethynyl-2-fluorobenzene | HCID 14618265 | — |
| Lösungsmittel | Pyridine methanol | HCID 22021344 | — |
| Produkt | 1,4-Diphenyl-1,3-butadiyne | HCID 70174 | 225,9% |
Reaktionsschritte
To a 50 ml round bottom flask equipped with a magnetic stirrer and reflux condenser was added 300 mg 4-decyloxy-3-fluorophenylacetylene and 43 mg cupric acetate in 40 ml 1:1 pyridine/MeOH. The reaction mixture was refluxed for 2 hrs, allowed to cool to room temperature and then added dropwise into a stirred 9 M aqueous sulfuric acid solution at ice bath temperature. The resulting cream-like suspension was extracted with ethyl ether and sequentially washed with water (3x) and brine and dried with anhydrous magnesium sulfate yielding 289 mg of a yellow-brown solid. Flash chromatography (1% ethyl acetate/hexane) and recrystallization of the residue from 95% ethanol afforded 248 mg diphenyldiacetylene (V), 4,4'-didecyloxy-3,3'-difluoro diphenyldiacetylene, as pale yellow needles.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05178791 |
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| Quelldatensatz | uspto-grants-1993_01 |
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| ORD ID | ord-b953cacb95fb49c589bf02db153921f6 |
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| Quellennotiz | uspto-grants-1993_01 |
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