Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2'-Bipyridine | HCID 1474 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cyclohexane diethylether | HCID 21895417 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Water | HCID 962 | — |
| Product | Bipyridine, polymer-bound | HCID 4613269 | 55.4% |
Reaction Steps
A solution of phenyllithium.cyclohexane/diethyl ether (40.9 ml, 38.4 mmol) was dropwise added to a mixture of 2,2′-bipyridine (5.0 g, 32.0 mmol) and diethyl ether (50 ml) at 5° C. while 15 minutes. This reaction mixture was stirred at room temperature for 2 hours, then the mixture was poured into water, an organic layer was separated from the mixture, furthermore an aqueous layer was extracted with dichloromethane. The organic layer was combined, and the solvent was distilled off, and the residue was diluted with acetone (50 ml), then saturated potassium permanganate acetone solution (120 ml) was added thereto, the mixture was stirred at room temperature for 1 hour. The obtained reaction mixture was filtered by Celite, the solvent of the filtrate was distilled off, and the residue was purified by silica gel column chromatography and recrystallization, thereby obtaining 4.2 g of 6-phenyl-2,2′-bipyridine as white crystal. Yield: 55.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442797B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-7964872ef94b4462aa6cb83eb4999bbc |
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| Source note | uspto-grants-2008_10 |
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