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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1485517생성일: 2026년 10월 27일

Dimethylformamide → 5-Bromo-2-chloro-3-nitropyridine

https://huagongshe.com/reaction/1485517

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Phosphorus oxychlorideHCID 24813—
반응물5-Bromo-3-nitro-2-pyridoneHCID 85147—
생성물5-Bromo-2-chloro-3-nitropyridineHCID 701941285%

반응 단계

To a solution of 5-bromo-3-nitropyridin-2(1H)-one (4.62 g, 21.10 mmol) in POCl3 (46.2 ml) was added DMF (4.62 ml, 59.7 mmol) at room temperature. The mixture was refluxed for 2 hours, and then cooled to room temperature and concentrated in vacuo. The residue was treated with saturated aq. NaHCO3 and extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by column chromatography on SiO2 (Hex:EtOAc=3:1) to give 5-bromo-2-chloro-3-nitropyridine (4.24 g, 85%) as a yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 8.37 (1H, d, J=2.4 Hz), 8.70 (1H, d, J=2.0 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09422298B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-ac60d0e5e6884b69b696ccae93017adc
출처 메모uspto-grants-2016_08