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HRID 1180258Erstellt: 26. Oktober 2026

1,3-Dibromo-5-fluorobenzene → 3'-Bromo-4,5'-difluorobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1180258

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-Dibromo-5-fluorobenzeneHCID 137003—
Edukt5-Fluoro-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 22180790—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt3'-Bromo-4,5'-difluorobiphenyl-2-carbonitrileHCID 179648419,4%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

5-Fluoro-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzonitrile (0.99 g, 4.0 mmol) and 1,3-dibromo-5-fluorobenzene (1.52 g, 6.0 mmol) were suspended in 1,2-dimethoxyethane (8 ml) and 2N sodium carbonate solution (4 ml) and degassed for 30 min before addition of tetrakis(triphenylphosphine)palladium(0). On complete addition the mixture was heated at 65° C. for 20 h. The mixture was partitioned between ethyl acetate (100 ml) and water (50 ml), the organic layer separated and washed with brine (50 ml), dried over anhydrous sodium sulphate, filtered and evaporated onto silica. The product was purified by flash column chromatography on silica, eluting with isohexane on a gradient of diethyl ether (5-100%). Combination of the desired fractions and evaporation gave 3′-bromo-4,5′-difluorobiphenyl-2-carbonitrile (110 mg, 9%) as a white solid: δH (500 Mfz, CDCl3) 7.53-7.55 (1H, m), 7.67 (1H, s), 7.69-7.76 (3H, m), 8.03 (1H, dd, J 9 and 2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07279580B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-e27e468424f041a391795dfdd250d5e1
Quellennotizuspto-grants-2007_10