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HRID 62033作成日:2026年10月23日

Cesium carbonate → 3-bromo-1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazole

https://huagongshe.com/ja/reaction/62033

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Benzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
反応物3-Bromo-1-(4-isopropoxyphenyl)-1H-1,2,4-triazoleHCID 118674678—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Dimethyl SulfoxideHCID 679—
生成物3-bromo-1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazoleHCID 9040430064%

反応条件

温度100 °C

反応手順

3-Bromo-1-(4-isopropoxyphenyl)-1H-1,2,4-triazole (7.15 g, 48.3 mmol), copper(I) iodide (1.25 g, 6.56 mmol), cesium carbonate (18.9 g, 58.0 mmol), and 1-iodo-4-(trifluoromethyl)benzene (8.29 g, 30.5 mmol) were added to dimethylsulfoxide (50 mL) and the solution was degassed with nitrogen for 10 minutes. The solution was heated at 100° C. for 20 hours. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate and filtered through Celite®. The resulting filter cake was rinsed with additional ethyl acetate (100 mL). Saturated aqueous ammonium chloride was added to the filtrate which was then stirred for 30 minutes. The layers were separated and the aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic extracts were dried over anhydrous magnesium sulfate and concentrated onto Celite®. Purification by silica gel chromatography using 0-100% ethyl acetate/hexanes as eluent provided the title compound as a white solid (5.64 g, 64%): mp 87-89° C.; 1H NMR (400 MHz, CDCl3) δ 8.53 (s, 1H), 7.85-7.77 (m, 4H); ESIMS m/z 292.0 ([M+H]+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09445594B2
出典データセットuspto-grants-2016_09
ORD IDord-665c7987de404b1abc01902c47a9b5a4
出典メモuspto-grants-2016_09