Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765104Generated: November 1, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 17975610, compound

https://huagongshe.com/reaction/1765104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassium FluorideHCID 522689—
Reactant2-Chloro-3-fluoropyridineHCID 2782791—
Reactant5-Fluoro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 22180790—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17975610HCID 1797561062.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a degassed solution of 5-fluoro-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzonitrile (5.55 g, 22.46 mmol), 2-chloro-3-fluoropyridine (2.95 g, 22.46 mmol), potassium fluoride (4.3 g, 74.14 mmol) and tris(dibenzylideneacetone)dipalladium(0) (0.824 g, 0.89 mmol) in THF (80 ml) and water (8 ml) was added tri(tert-butyl)phosphine (0.51M solution in hexane; 3.52 ml, 1.79 mmol). The reaction was heated at 70° C. for 48 h, then allowed to cool to ambient temperature. The reaction mixture was filtered through a catalyst filter, and the filtrate diluted with ethyl acetate (400 ml) and washed with water (2×100 ml). The organic phase was separated, dried (MgSO4), filtered and adsorbed onto silica gel. The crude product was chromatographed on silica, eluting with 10% ethyl acetate in isohexane, to give 5-fluoro-2-(3-fluoropyridin-2-yl)benzonitrile as a white solid (3.02 g): δH (400 MHz, CDCl3) 7.40-7.45 (2H, m), 7.51-7.61 (2H, m), 7.72-7.76 (1H, m), 8.58-8.60 (1H, m); m/z (ES+) 217.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226926B2
Source datasetuspto-grants-2007_06
ORD IDord-1a6bdad1287d476d9d5a785fd0ed2f25
Source noteuspto-grants-2007_06