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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2229538생성일: 2026년 10월 26일

Sodium Hydroxide → 5-Trifluoromethoxysalicylic acid

https://huagongshe.com/reaction/2229538

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-Hydroxy-5-(trifluoromethoxy)benzaldehydeHCID 1268058—
촉매Silver NitrateHCID 24470—
용매WaterHCID 962—
생성물5-Trifluoromethoxysalicylic acidHCID 277510391%

반응 단계

To a stirring solution of NaOH (8.15 g, 203.8 mmol) in water (35 mL, 5.8 M) was added an aq solution of silver nitrate (17.3 g, 101.9 mmol, 35 mL water, 2.9 M). A brownish solid formed. The flask was placed in an ice bath and to the stirring suspension was added 2-hydroxy-5-trifluoromethoxy-benzaldehyde in 500 mg portions (10.0 g, 48.5 mmol). After addition was complete and the reaction was stirred for 10 min in an ice bath, the mixture was filtered and the brownish precipitate was washed with hot water. The combined washings were acidified with conc HCl to pH 1 and the precipitate was collected by vacuum filtration. This solid was then dissolved in ethyl acetate. The ethyl acetate was washed with saturated aq NaCl, dried over Na2SO4, and filtered. The aqueous layer was also extracted with ethyl acetate. This organic layer was washed with saturated aq NaCl, dried over Na2SO4, filtered and concentrated to provide 2-hydroxy-5-trifluoromethoxy-benzoic acid (9.8 g, 91%) as a white solid: Rf 0.38 (20% methanol in dichloromethane); 1H NMR (CDCl3, 300 MHz) δ 10.30 (bs, 1H), 7.79 (d, J=3.0 Hz, 1H), 7.41 (dd, J1=9.3 Hz, J2=3.0 Hz, 1H), 7.05 (d, J=9.0 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06420426B1
출처 데이터셋uspto-grants-2002_07
ORD IDord-c9df3e4ba3b8434893bb7529697a246d
출처 메모uspto-grants-2002_07