Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183994Generated: October 26, 2026

Tris(1,1-dimethylethyl)phosphine → 3'-Amino-4,2',6'-trifluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/2183994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassium FluorideHCID 522689—
Reactant3-Bromo-2,4-difluoroanilineHCID 13732746—
Reactant5-Fluoro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 22180790—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
Product3'-Amino-4,2',6'-trifluorobiphenyl-2-carbonitrileHCID 22240097106.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 3-bromo-2,4-difluorophenylamine (5.2 g, 25 mmol) and 5-fluoro-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzonitrile (7.10 g, 28.8 mmol) in tetrahydrofuran (95 ml) and water (5 ml) was treated with potassium fluoride (4.8 g, 82.5 mmol) and this mixture was degassed with nitrogen for 10 min before adding tris(dibenzylideneacetone)dipalladium(0) (460 mg, 0.5 mmol) and tri-tert-butylphosphine (2.5 ml of a 0.2M solution in 1,4-dioxane, 0.5 mmol). The reaction was then heated at 50° C. for 2 h then cooled to ambient temperature. The mixture was poured into ice-cold 0.5N sodium hydroxide (750 ml), stirred for 10 min and the solid collected by filtration. This was triturated with water and dried to afford 3′-amino-4,2′,6′-trifluorobiphenyl-2-carbonitrile as a grey powder (6.6 g). Used without further purification: δH (360 MHz, CDCl3) 3.74 (2H, br), 6.79-6.89 (2H, m), 7.36-7.42 (1H, m), 7.45-7.51 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-514f226fdce646a5847069c64f96fd75
Source noteuspto-grants-2005_05