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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 722340생성일: 2026년 10월 23일

Acetic Acid → 2-amino-5-(trifluoromethoxy)benzoic Acid

https://huagongshe.com/ko/reaction/722340

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrogen PeroxideHCID 784—
반응물Potassium HydroxideHCID 14797—
반응물5-(trifluoromethoxy)-2,3-dihydro-1H-indole-2,3-dioneHCID 2732752—
용매WaterHCID 962—
생성물2-amino-5-(trifluoromethoxy)benzoic AcidHCID 1108534987%

반응 조건

온도0 °C

반응 단계

5-(Trifluoromethoxy)isatin (15.0 g, 65 mmol) and potassium hydroxide pellets (4 g) were mixed in water (35 mL) and cooled to 0° C. With vigorous stirring, a solution of 30% aqueous hydrogen peroxide (11.7 g), potassium hydroxide pellets (5.8 g), and water (80 mL) was added drop-wise keeping the temperature below 10° C. After stirring 1 hour at 0° C., glacial acetic acid (22 mL) was added drop-wise, causing foaming and formation of a precipitate. The contents were stirred overnight and filtered to afford the 2-amino-5-trifluoromethoxybenzoic acid as an amber solid (12.5 g, 87%). A small amount was recrystallized from ethyl acetate-hexanes to afford amber needles for an analytical sample and the remaining compound was used without further purification: mp 142.5–144.2° C. 1H NMR (CDCl3, 300 MHz) 7.98 (s, 1H), 7.18 (d, 1H, J=8.0 Hz) 6.62 (d, 1H, J=8.0 Hz), 6.40 (brs, 2H). Anal. Calc'd for C8H6NO3F3: C, 43.45; H, 2.73; N, 6.33. Found: C, 43.40; H, 2.65; N, 6.35.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07138411B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-0a92c2dfede9405790d56cf16661bad2
출처 메모uspto-grants-2006_11