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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62033생성일: 2026년 10월 24일

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

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

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Benzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
반응물3-Bromo-1-(4-isopropoxyphenyl)-1H-1,2,4-triazoleHCID 118674678—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
생성물3-bromo-1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazoleHCID 9040430064%

반응 조건

온도100 °C

반응 단계

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]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09445594B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-665c7987de404b1abc01902c47a9b5a4
출처 메모uspto-grants-2016_09