돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341680생성일: 2026년 10월 26일

Hydrogen Bromide → 4-Bromo-4'-chloro-3-methylbiphenyl

https://huagongshe.com/reaction/341680

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물AcetonitrileHCID 6342—
반응물Butyl nitriteHCID 10996—
반응물4'-Chloro-3-methylbiphen-4-ylamineHCID 23005188—
촉매copper(I) bromideHCID 24593—
생성물4-Bromo-4'-chloro-3-methylbiphenylHCID 59450516—

반응 단계

4′-Chloro-3-methylbiphen-4-ylamine (16.5 g, 0.077 mol) is added to acetonitrile (140 ml) and stirred at room temperature until dissolution is complete. The reaction mixture is cooled to between −5° C. and 0° C., tent-butyl nitrite (90%, 12.4 ml, 0.093 mol) is added dropwise and the reaction mixture is maintained at between −5° C. and 0° C. for 30-40 minutes. The mixture is added slowly to a preheated (50° C.) suspension of copper (I) bromide (5.8 g, 0.04 mol) in hydrobromic acid (5.8 ml) and stirred at 50° C. for 10-15 minutes. The reaction mixture is cooled to room temperature, then poured into ice-cold water and extracted with ethyl acetate (3×300 ml). The organic extracts are washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to yield 4-bromo-4′-chloro-3-methylbiphenyl (11.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895761B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-bfcdb1d490d340b3aa4b2dd6faffe227
출처 메모uspto-grants-2014_11