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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62053생성일: 2026년 10월 24일

Lithium Hydroxide → 2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetic acid

https://huagongshe.com/ko/reaction/62053

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HydroxideHCID 3939—
반응물methyl 2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetateHCID 90405381—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetic acidHCID 9040421798.5%

반응 단계

In a 100 mL flask, methyl 2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetate (3.45 g, 9.14 mmol) and lithium hydroxide.hydrate (1.15 g, 27.4 mmol) were diluted with tetrahydrofuran (24.4 mL), methanol (24.4 mL), water (12.2 mL). The reaction was stirred at room temperature for 2 hours. The solvent was evaporated and the resulting solid was diluted with water and adjusted to pH 3 with hydrogen chloride (1 N). The resulting precipitate was extracted with ethyl acetate (5×100 mL). The combined organics were dried over magnesium sulfate, filtered, and concentrated to give the title compound as a white solid (3.27 g, 96%): 1H NMR (400 MHz, DMSO-d6) δ 12.41 (s, 1H), 9.40 (s, 1H), 8.15-8.03 (m, 4H), 7.63 (dq, J=7.9, 1.0 Hz, 2H), 7.49-7.36 (m, 2H), 3.66 (s, 2H), 3.35 (s, 3H); 19F NMR (376 MHz, DMSO-d6) δ −56.98; ESIMS m/z 364 ([M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09445594B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-8de628aad8cd472a84cf4e430d314bd6
출처 메모uspto-grants-2016_09