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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334586생성일: 2026년 10월 24일

Hydrogen Bromide → 3-Bromo-2-nitroanisole

https://huagongshe.com/ko/reaction/334586

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물Sodium BicarbonateHCID 516892—
반응물3-Methoxy-2-nitroanilineHCID 10464700—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물3-Bromo-2-nitroanisoleHCID 25873497%

반응 조건

온도0 °C

반응 단계

3-Methoxy-2-nitro-phenylamine (360 mg, 2.14 mmol) was dissolved in HBr (48%, 4.8 mL) at 0° C. A solution of sodium nitrite (0.16 g, 2.40 mmol) in water (360 μL) was added dropwise to the stirred solution over one hour period while the temperature was maintained at 0° C. Then a cold (0° C.) freshly prepared solution of CuBr2 (from CuSO4.5H2O (1.0 g) and HBr (48%, 1.0 mL) mixed 30 min. at room temperature to give a dark purple solution) was added at 0° C. to the reaction mixture. The resulting solution was stirred at 0° C. for 3 hours and at room temperature for 2 days. The reaction mixture was poured onto ice and neutralized carefully with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The resulting organic phase was washed with brine, dried over MgSO4, filtered and evaporated to yield 482 mg (2.08 mmol, 97%) of 1-bromo-3-methoxy-2-nitrobenzene as an orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883826B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-65acff0a11414b3e8bd27753ad3acb24
출처 메모uspto-grants-2014_11