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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924938Generated: October 27, 2026

4-Bromobiphenyl → 1-(1,1'-Biphenyl)-4-yl-2-phenylethan-1-one

https://huagongshe.com/reaction/924938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobiphenylHCID 7101—
Reactant2-(3-Methylphenyl)acetophenoneHCID 13173614—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(1,1'-Biphenyl)-4-yl-2-phenylethan-1-oneHCID 7481724%

Reaction Steps

To a solution of 4-bromobiphenyl (683 mg, 2.9 mmol) in anhydrous THF (5 mL) was added n-BuLi (1.2 mL, 2.9 mmol) dropwise at −78° C. After being stirred at the temperature for 0.5 h, a solution of N-methoxy-N-methyl-2-phenyl-acetamide (prepared following step 1 of Intermediate 4) (500 mg, 2.8 mmol) in anhydrous THF (5 mL) was added via a syringe, and the mixture was stirred at −78° C. for 2 h. The reaction was quenched with saturated NH4Cl aqueous solution, and extracted with EtOAc. The organic layer was dried over Na2SO4, concentrated in vacuo, and purified by column chromatography (PE:EtOAc=20:1) to give 1-(biphenyl-4-yl)-2-phenylethanone (180 mg, yield 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283229B2
Source datasetuspto-grants-2016_03
ORD IDord-cdd19428d3154f77974e384f5be451fd
Source noteuspto-grants-2016_03