Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobiphenyl | HCID 7101 | — |
| Reactant | 2,6-diphenylaniline | HCID 11010226 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 86762384 | HCID 86762384 | 471.7% |
Reaction Steps
Xylene (250 mL) was bubbled with nitrogen for 15 min, followed by addition of 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (4.6 g, 11.2 mmol) and Pd2(dba)3 (2.6 g, 2.8 mmol). The mixture was bubbled with nitrogen for 15 min, then [1,1′:3′,1″-terphenyl]-2′-amine (13.7 g, 56.0 mmol), 4-bromobiphenyl (13.0 g, 56.0 mmol), sodium tert-butoxide (10.8 g, 112.0 mmol) were added. The mixture was bubbled with nitrogen for 15 min and refluxed for 12 h. After cooling, the reaction mixture was filtered through a silica pad and washed with toluene. The solvent was removed in vacuo and the residue was purified by flash chromatography using 30-40% toluene/hexane to afford N-([1,1′-biphenyl]-4-yl)-[1,1′:3′,1″-terphenyl]-2′-amine (21.0 g, 93% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716484B1 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-359e52bcfd01480f961ed9816339ce3e |
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| Source note | uspto-grants-2014_05 |
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