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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064264Generated: October 30, 2026

2-Bromo-5-fluorobenzonitrile → 5'-Acetyl-4,2'-difluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1064264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-fluorobenzonitrileHCID 93654—
ReactantPotassium FluorideHCID 522689—
Reactant1-(4-Fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethan-1-oneHCID 22273592—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product5'-Acetyl-4,2'-difluorobiphenyl-2-carbonitrileHCID 2227359958.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a degassed solution of 1-[4-fluoro-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]ethanone (12 g, 45.43 mmol), 2-bromo-5-fluorobenzonitrile (9.09 g, 5.28 ml, 45.44 mmol), potassium fluoride (7.92 g, 136.31 mmol) and tris(dibenzylideneacetone)palladium(0) (0.834 g, 0.908 mmol) in THF (200 ml) and water (10 ml) was added tri-tert butylphosphine (10% weight solution) (0.368 g, 3.63 ml, 1.817 mmol). The reaction was heated at 70° C. for 14 h then allowed to cool to ambient temperature. The reaction was partitioned between water (200 ml) and ether (300 ml). The aqueous phase was extracted with ether (150 ml) and the combined organics washed with brine (200 ml), dried (MgSO4), filtered and evaporated to give a brown solid. The solid was dissolved in DCM and adsorbed onto silica. The crude product was chromatographed on silica (5-20% EtOAc in isohexane) to give the title product as a white solid (6.8 g): δH (400 MHz, CDCl3) 2.63 (3H, s), 7.31 (1H, t, J 9.0 Hz), 7.40-7.44 (1H, m), 7.50-7.53 (2H, m), 8.02-8.10 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969716B2
Source datasetuspto-grants-2005_11
ORD IDord-13bb162f9eca4037acf08c41805da85d
Source noteuspto-grants-2005_11