Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbazole | HCID 6854 | — |
| Reactant | 4,4'-Dibromobiphenyl | HCID 7110 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58013136 | HCID 58013136 | 6.9% |
Reaction Steps
Carbazole (1.80 g, 10.9 mmol), 4,4′-dibromobiphenyl (0.75 g, 2.4 mmol), and potassium tbutoxide (2.24 g, 20 mmol) were dissolved in dry toluene and heated at 135° C. for 24 h. The solution was filtered and the solvent was removed in vacuo, the residue was dry-packed on SiO2 and chromatographed using 10% acetone in hexanes to afford (0.08 g, 6%) of the product. 1H NMR (CDCl3) δ 8.22-8.16 (m, 4H), 7.93-7.65 (m, 8H), 7.56-7.49 (m, 8H), 7.47-7.28 (m, 4H). 13C NMR (CDCl3+DMSO-d6) δ 142.1, 140.8, 140.7, 139.0, 138.3, 137.3, 130.5, 128.5, 127.3, 126.1, 126.0, 125.9, 125.6, 123.4, 120.3, 120.2, 120.0, 109.7. EI MS m/z 484 [M+], m.p.=244-246° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785002B1 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-15ac434f2d794cdc80d9a448a376691a |
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| Source note | uspto-grants-2014_07 |
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