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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 887287생성일: 2026년 10월 26일

Hydrogen Bromide → 3-Bromo-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/887287

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물UreaHCID 1176—
반응물Sodium HydroxideHCID 14798—
반응물3-Amino-4-(trifluoromethyl)benzoic acidHCID 642651—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물3-Bromo-4-(trifluoromethyl)benzoic acidHCID 22337570—

반응 조건

온도75 °C

반응 단계

3-Amino-4-trifluoromethylbenzoic acid (8.20 g, 40.0 mmol), prepared according to Astrid Giencke and Helmut Lackner, Liebigs Ann. Chem., 569-579:6 (1990), in 48% HBr (20 mL) and H2O (67 mL) at 0° C. was treated with NaNO2 (2.99 g) in small portions over 15 minutes. After stirring for 30 minutes, the mixture was treated with urea (0.250 g) and then the mixture was added dropwise to a solution of CuBr (10.0 g) in 48% HBr (40 mL) and H2O (100 mL). The reaction mixture was heated at 75° C., stirred for 2 hours, cooled to room temperature, and stirred overnight. The mixture was treated with 20% NaOH until the pH>10. The resulting blue copper salts were removed by filtration through Celite. The mixture was acidified to pH 1 with HCl, extracted with CH2Cl2 (3×200 mL), dried over Na2SO4, filtered, and the filtrate was concentrated under reduced pressure to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247413B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-3f7c81b28cc94f25a91d4bda91786269
출처 메모uspto-grants-2012_08