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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037648Generated: November 1, 2026

Benzophenone → HCID 10830973, compound

https://huagongshe.com/reaction/1037648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
Reactant2,6-DibromopyridineHCID 12274—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10830973HCID 1083097335%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546501B2
Source datasetuspto-grants-2013_10
ORD IDord-f1bd899a30444c98a7c23d57826b8c1f
Source noteuspto-grants-2013_10