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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1421516생성일: 2026년 10월 25일

Ethanol → 3-Ethoxy-5-[4-(trifluoromethyl)phenyl]-4H-1,2,4-triazole

https://huagongshe.com/reaction/1421516

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Potassium HydroxideHCID 14797—
반응물Potassium BromideHCID 253877—
반응물5-[4-(Trifluoromethyl)phenyl]-1,3,4-oxadiazol-2-amineHCID 5216085—
용매Acetic AcidHCID 176—
생성물3-Ethoxy-5-[4-(trifluoromethyl)phenyl]-4H-1,2,4-triazoleHCID 178467488—

반응 조건

온도24 °C

반응 단계

5-[4-(Trifluoromethyl)phenyl]1,3,4-oxadiazol-2-amine (10 g, 44 mmol) and potassium hydroxide (7.4 g, 0.132 mol) dissoved in abs. ethanol (300 ml) were heated at reflux for 3 h. After being cooled to 24° C., the solution was neutralized with acetic acid and concentrated by rotary evaporation. The residue was taken up in ethyl acetate and washed with water and brine. Recrystallization from acetonitrile/ether (2:1) gave 9 g (82%); mp 151-152° C.; IR(KBr, υ=cm-1) 2996, 1534, 1460, 1330, 1162, 1130, 1070; 1H NMR (300 MHz, DMSO-d6) δ 1.35 (3H, t, J=7.1 Hz), 4.38 (2H, q, J=7.0 Hz), 7.82 (2H, d, J=8.3 Hz), 8.10 (2H, d, J=8.1 Hz), 13.64 (1H, br. s); MS(DCl)m/z: 258 (MH+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06077861
출처 데이터셋uspto-grants-2000_06
ORD IDord-69af224711d946e2834e454383a0c8a0
출처 메모uspto-grants-2000_06