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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374109Generated: November 3, 2026

Benzophenone → diphenyl-(2-phenylphenyl)methanol

https://huagongshe.com/reaction/2374109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
Reactant2-BromobiphenylHCID 16329—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Productdiphenyl-(2-phenylphenyl)methanolHCID 410659—

Reaction Steps

α,α-Diphenyl-2-biphenylmethanol was prepared by the following procedure (Reaction Scheme 1). To a solution of 2-bromobiphenyl (5.00 g, 21.45 mmol) in freshly distilled THF (50 mL) at −78° C. was added n-BuLi (1.37 g, 21.45 mmol, 8.6 mL of 2.5 M solution in hexanes) dropwise via syringe. Approximately 5 minutes after complete addition, benzophenone (4.10 g, 22.52 mmol) was added in a single portion, after which time the ice bath was removed and the solution allowed to warm to room temperature. After 2 h, the reaction was quenched with the addition of NH4Cl and H2O (100 mL), and extracted with Et2O (3×100 mL). The combined organic layers were washed with brine, dried over MgSO4, and concentrated to dryness. Chromatography gave the product as a white solid (6.27 g, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462405B2
Source datasetuspto-grants-2008_12
ORD IDord-2ce7cecdadc443838848401fb13f1e3b
Source noteuspto-grants-2008_12