Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 86629340 | HCID 86629340 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86101308 | HCID 86101308 | — |
Reaction Steps
A mixed solution of 0.61 g of 2-[1-(4-t-butylphenyl)pyren-7-yl]-4,4,5,5-tetramethyl 1,3,2-dioxaborolane, 0.28 mL of bromobenzene, 1.2 g of tripotassium phosphate, 0.18 g of tetrabutylammonium bromide, 14 mg of palladium acetate and 15 mL of dimethylformamide was heated and stirred under a nitrogen gas stream at 130° C. for 8 hours. The solution was cooled to room temperature and poured into 75 mL of water, and then the precipitated solid was collected by filtration. The resulting solid was dissolved in dichloromethane, washed with water, dried over magnesium sulfate and then concentrated. The resulting crude product was purified by column chromatography and then vacuum-dried to obtain 0.49 g of 1-(4-t-butylphenyl)-7-phenylpyrene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08610345B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-42d16eec4fd94a7db2b6b3de8a4deeff |
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| Source note | uspto-grants-2013_12 |
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