Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10830973 | HCID 10830973 | 35% |
Reaction Steps
At −78° C. a 2.5 M solution of n-butyl lithium in hexanes (18.6 mL, 46.4 mmol, 1.1 equiv) was added dropwise to 2,6-dibromopyridine (1) (10.0 g, 42.2 mmol, 1.0 equiv) in THF (780 mL). The solution was then stirred for 20 min at which point benzophenone (8.07 g, 44.3 mmol, 1.05 equiv) was added. The reaction was allowed to stir an additional 0.5 hr at −78° C., at this time the cooling bath was removed and the reaction allowed to warm room temperature. The reaction was stirred at room temperature for 1 hr and quenched with saturated sodium bicarbonate (250 mL). The layers were separated and the aqueous layer extracted with dichloromethane (250 mL). The combined organic layers were dried over sodium sulfate and absorbed onto silica gel (30 g) by concentration under reduced pressure. This material was then purified on a silica gel column (300 g) by eluting with heptanes (2 L), ethyl acetate (2%) in heptanes (2 L) and finally ethyl acetate (5%) in heptanes (2 L). The desired product was isolated pure in 35% yield (5.0 g). A second fraction (5.4 g) of product and benzophenone was also isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546501B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f1bd899a30444c98a7c23d57826b8c1f |
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| Source note | uspto-grants-2013_10 |
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