戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 243875作成日:2026年10月26日

Sodium Bicarbonate → 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile

https://huagongshe.com/reaction/243875

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物2-Bromo-3-fluorobenzonitrileHCID 2783393—
反応物1H-Pyrazole-5-boronic acidHCID 11251979—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物3-fluoro-2-(1H-pyrazol-5-yl)benzonitrileHCID 6711692820.7%

反応条件

温度23 °C

反応手順

2-Bromo-3-fluorobenzonitrile (1.0 g, 5.0 mmol) and (1H-pyrazol-5-yl)boronic acid (647 mg, 4.6 mmol) were combined and dissolved in degassed DME (15 mL) then treated with NaHCO3 (1260 mg, 8.4 mmol) in water and the reaction purged with bubbling N2 for 5 minutes. The reaction was treated with Pd(PPh3)4 (288 mg, 0.2 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated to reflux for 2 h. The reaction was then cooled to 23° C. filtered and the solids were rinsed with EtOAc and the layers separated. The organic layers were combined, dried and concentrated under reduced pressure. Chromatography (0-30% ethyl acatate/hexanes) afforded 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile (178 mg, 19%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653263B2
出典データセットuspto-grants-2014_02
ORD IDord-a08601227d3d4cc4a757065d38125524
出典メモuspto-grants-2014_02