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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42540생성일: 2026년 10월 24일

Hydrogen Bromide → 3-Bromo-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/ko/reaction/42540

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참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물3-Amino-5-(methoxycarbonyl)benzoic acidHCID 13557643—
반응물Sodium NitriteHCID 23668193—
생성물3-Bromo-5-(methoxycarbonyl)benzoic acidHCID 2259364168%

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온도0 °C

반응 단계

3-Amino-5-(methoxycarbonyl)benzoic acid (1.0 g, 5.12 mmol, 1 eq.) was dissolved in 15% HBr (22.5 mL) at RT, then cooled to 0° C. with stirring. A 2.5 M aqueous solution of NaNO2 (2.3 mL, 5.64 mmol, 1.1 eq.) was added slowly via an addition funnel to generate the diazonium salt. In a separate flask, CuBr was partially dissolved in 15% HBr (9 mL) and cooled to 0° C. with stirring, to which the diazonium salt solution was subsequently added. A slight exotherm was observed. The reaction was stirred at RT for 30 minutes then carefully heated at 70° C. for 1 hour. The reaction was worked up by filtering off insoluble material as crude product. The solids were dissolved in water/EtOAc and the layers separated. The aqueous layer was extracted again with EtOAc. The organic layers were combined, dried over sodium sulfate and concentrated to give an off-white solid. The product was purified over silica gel in 1:1 hexanes/EtOAc to 100% EtOAc to 4:1 methylene chloride/MeOH to yield 3-bromo-5-(methoxycarbonyl)benzoic acid (0.90 g, 3.47 mmol, 68% yield) as a white solid. MS found: (M−H)+=257/259.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536198B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-3e613da65351428bb2c345652ac97ce7
출처 메모uspto-grants-2013_09