Reaktionsgleichung
C(O[C:12]1[CH:17]=[CH:16][C:15]([C:18]#[CH:19])=[CH:14][C:13]=1F)CCCCCCCCC.S(=O)(=O)(O)O>N1C=CC=CC=1.CO>[CH:12]1[CH:13]=[CH:14][C:15]([C:18]#[C:19][C:19]#[C:18][C:15]2[CH:14]=[CH:13][CH:12]=[CH:17][CH:16]=2)=[CH:16][CH:17]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
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 9M aqueous sulfuric acid solution at ice bath temperature. The resulting cream-like suspension was extracted with ethyl ether and sequentially washed with water (3×) 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 (5), 4,4'-didecyloxy-3,3'-difluoro diphenyldiacetylene, as pale yellow needles.
Aufarbeitung
- customTo a 50 ml round bottom flask equipped with a magnetic stirrer
- temperaturereflux condenser
- temperatureThe reaction mixture was refluxed for 2 hrs
- extractionThe resulting cream-like suspension was extracted with ethyl ether
- washsequentially washed with water (3×) and brine
- dry with materialdried with anhydrous magnesium sulfate yielding 289 mg of a yellow-brown solid
- customFlash chromatography (1% ethyl acetate/hexane) and recrystallization of the residue from 95% ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-900166b49b4a4248952022f9db303171
- Quelldatensatz
- uspto-grants-1995_10
- Patentnummer
- US05457235
Verknüpfte Notizen
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