돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30874생성일: 2026년 10월 25일

Pyridiniumtribromide → 2-Bromo-1-(3-methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanone

https://huagongshe.com/reaction/30874

반응식

참여 물질

역할이름HCID투입량
반응물PyridiniumtribromideHCID 21124087—
반응물1-(3-Methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanoneHCID 21985798—
용매Acetic AcidHCID 176—
생성물2-Bromo-1-(3-methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanoneHCID 2198568859%

반응 조건

온도110 °C

반응 단계

A mixture of 1-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)ethanone (5.66 g, 22 mmol), pyridinium tribromide (10.63 g, 33.0 mmol), and glacial acetic acid (60 mL) was stirred at 110° C. for 3 h. The reaction mixture was cooled to 0-5° C., and the precipitated product was collected by filtration and washed with small amounts of water, ethanol, and diethyl ether. The crude material was purified by flash chromatography (5:95 ethyl acetate/hexane) to give 2-bromo-1-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)ethanone as a light yellow solid (4.33 g, 59% yield). HPLC ret. time 3.63 min; 1H NMR (CDCl3) δ: 2.63 (s, 3H), 2.25 (s, 2H), 7.52-7.58 (m, 2H), 7.72-7.83 (m, 3H), 8.32 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423156B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-13f279f0c2114ca1b1c429ba8eb11603
출처 메모uspto-grants-2008_09