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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2209521생성일: 2026년 10월 24일

Hydrochloric Acid → 3-carboxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone

https://huagongshe.com/ko/reaction/2209521

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물3-carboethoxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinoloneHCID 19958905—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물3-carboxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinoloneHCID 1995890431.6%

반응 조건

온도90 °C

반응 단계

A suspension of 3-carboethoxy-2-trifluoromethyl-2-hydroxy-4(3-nitrophenyl)-2,3,4,6,7,8-hexahydro-5(1H)-quinolone (7.02 g) in ethanol (40 ml) and water (40 ml) was treated with lithium hydroxide monohydrate (1.44 g). The mixture was heated at 90° C. for 30 minutes, diluted with water, acidified with 1N hydrochloric acid, and extracted with ethyl acetate. The combined organic extracts were washed (water and brine), dried, filtered and the solvent stripped to yield a brown oil which was further purified by chromatography (ethyl acetate and ethyl acetate/methanol, 4:1). 3-Carboxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone (2.07 g) was obtained as a white solid. NMR: 1.85 (m,2, CH2), 2.10 (m,2, CH2), 2.33-2.60 (m,3, CH2, CH), 4.21 (d,1, J=8.7, CH), 7.47 (m,2, Ar), 7.81 (s,2, OH or NH, Ar), 7.96 (m,1H, Ar); MS: m/z=400(M).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05455253
출처 데이터셋uspto-grants-1995_10
ORD IDord-480c93e1370342d0b56c3245b2a02056
출처 메모uspto-grants-1995_10