HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374109Generated: November 3, 2026
Benzophenone → diphenyl-(2-phenylphenyl)methanol
https://huagongshe.com/reaction/2374109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | 2-Bromobiphenyl | HCID 16329 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | diphenyl-(2-phenylphenyl)methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462405B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-2ce7cecdadc443838848401fb13f1e3b |
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| Source note | uspto-grants-2008_12 |
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