Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-(Decyloxy)-4-ethynyl-2-fluorobenzene | HCID 14618265 | — |
| Solvent | Pyridine methanol | HCID 22021344 | — |
| Product | 1,4-Diphenyl-1,3-butadiyne | HCID 70174 | 225.9% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05457235 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-900166b49b4a4248952022f9db303171 |
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| Source note | uspto-grants-1995_10 |
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