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HRID 1945063作成日:2026年10月25日

Potassium Carbonate → 2-(3'-Chloro-3-fluorobiphenyl-4-yl)acetonitrile

https://huagongshe.com/reaction/1945063

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物(3-Chlorophenyl)boronic acidHCID 2734323—
反応物2-(4-Bromo-2-fluorophenyl)acetonitrileHCID 7172308—
触媒Tetrabutylammonium BromideHCID 74236—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3'-Chloro-3-fluorobiphenyl-4-yl)acetonitrileHCID 5960779687.6%

反応条件

温度70 °C

反応手順

A suspension of 4-bromo-2-fluorobenzyl cyanide (3.50 g, 16.35 mmol), 3-chlorobenzeneboronic acid (2.68 g, 17.17 mmol), Pd(OAc)2 (0.110 g, 0.491 mmol), K2CO3 (5.65 g, 40.9 mmol) and tetrabutylammonium bromide (5.80 g, 17.99 mmol) in water (14 ml) is allowed to stir under nitrogen at 70° C. for 1 hour. The reaction mixture is cooled to room temperature, and diluted with EtOAc. The two phases are separated. The organic layer is washed with brine, dried over MgSO4, filtered and concentrated. The obtained residue is purified by silica gel flash column chromatography (heptane/EtOAc=100:0 to 70:30) to give 2-(3′-chloro-3-fluorobiphenyl-4-yl)acetonitrile (3.52 g); HPLC retention time=1.17 minutes (condition B); 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 3.81 (s, 2H) 7.29-7.45 (m, 5H) 7.50-7.55 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394853B2
出典データセットuspto-grants-2013_03
ORD IDord-3ba72b0e79a54e1295ed40c57b222bdd
出典メモuspto-grants-2013_03