戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 240776作成日:2026年10月25日

Potassium Carbonate → 5-(1-Benzyl-1H-pyrazol-4-yl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/240776

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1,4-DioxaneHCID 31275—
反応物5-Bromo-2-fluorobenzonitrileHCID 2724900—
反応物1-Benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2734771—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物5-(1-Benzyl-1H-pyrazol-4-yl)-2-fluorobenzonitrileHCID 68723688—

反応条件

温度110 °C

反応手順

5-Bromo-2-fluorobenzonitrile (484 mg, 2.42 mmol), 1-benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (736 mg, 2.59 mmol), dichlorobis(triphenylphosphine)palladium(II) (174 mg, 0.248 mmol), and potassium carbonate (1.36 g, 9.84 mmol) were combined in a sealed vial with dioxane (10 mL) and water (1 mL) under an inert atmosphere of nitrogen, and the mixture was heated to 110° C. overnight. The mixture was diluted with methylene chloride and washed with water. The organic layer was absorbed on silica gel and purified by silica gel chromatography eluting with a gradient of 10-50% ethyl acetate in hexanes to afford the title compound. MS (ESI+) m/z 290.0 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08648069B2
出典データセットuspto-grants-2014_02
ORD IDord-e5612ec6eaa84a529192962f8ea3aec9
出典メモuspto-grants-2014_02