Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobiphenyl | HCID 7101 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 67336204 | HCID 67336204 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67337164 | HCID 67337164 | 71% |
Reaction Steps
Under a stream of argon, 2.8 ml of a hexane solution containing 4.3 mmol of butyl lithium was slowly added to 15 ml of tetrahydrofuran cooled to −78° C. in which prepared by dissolving 0.91 g of 4-bromobiphenyl. After stirring at −78° C. for 15 minutes, 1.19 g of dichloro(tetramethylethylenediamine)zinc(II) was added thereto and stirred at −78° C. for 10 minutes and then at room temperature for 2 hours. A 1.47 g portion of 2-(4-bromophenyl)-4,6-bis(1-naphthyl)-1,3,5-triazine prepared in Reference Example 4 and 0.14 g of tetrakis(triphenylphosphine)palladium(0) were dissolved in 80 ml of tetrahydrofuran and added to this solution, followed by stirring under heating reflux for 13 hours. The reaction solution was concentrated under a reduced pressure and the thus obtained solid was washed with chloroform to obtain a white solid of the intended 2,4-bis(1-naphthyl)-6-[1,1′:4′,1″]terphenyl-4-yl-1,3,5-triazine (1.19 g, yield 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994316B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-e7b83c1657e7429d848f5e5a8a24827d |
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| Source note | uspto-grants-2011_08 |
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