돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245144생성일: 2026년 10월 24일

Hydrochloric Acid → 6-Bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

https://huagongshe.com/ko/reaction/245144

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물5-BromoisatinHCID 6889—
반응물Potassium HydroxideHCID 14797—
반응물Propiophenone, 3'-(trifluoromethyl)HCID 137064—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Water ethanolHCID 19096565—
생성물6-Bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acidHCID 6738399587.2%

반응 조건

온도20 °C

반응 단계

5-Bromoisatin (198 g, 788 mmol) was dissolved in ethanol (1.2 L) in a 6 L conical jacketed lab reactor equipped with a mechanical stirrer and an internal temperature probe. A solution of KOH (265 g, 4730 mmol) in water (0.480 L) was added slowly via addition funnel over ca. 1 hour, such that the vessel temperature was maintained at 20° C. 1-[3-(Trifluoromethyl)phenyl]-1-propanone (159 g, 788 mmol) was added in one portion and the reactor was heated to reflux for 1 h. The reaction mixture was cooled to 20° C. and acidified to pH˜2 by addition of 450 mL of concentrated HCl. An additional 1.5 L of 50% EtOH/H2O was added to facilitate filtration. The slurry was filtered and the filter cake was rinsed twice with 1 L portions of 50% EtOH/water. The solid was dried in vacuo to give 6-bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (281.7 g, 87% yield) as a fine off-white solid. MS (m/z) 412.7 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658636B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-45b06bc08fc74b0da5c9182f1b0d29db
출처 메모uspto-grants-2014_02