돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1107287생성일: 2026년 10월 26일

Bromine → 4-(3-Bromo-4-methoxyphenyl)pyridine

https://huagongshe.com/reaction/1107287

반응식

참여 물질

역할이름HCID투입량
반응물BromineHCID 24408—
반응물4-(4-Methoxyphenyl)pyridineHCID 603813—
촉매IronHCID 23925—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물4-(3-Bromo-4-methoxyphenyl)pyridineHCID 18476096—

반응 조건

온도60 °C

반응 단계

4-(4-Methoxyphenyl)pyridine (1 g, 5.4 mmol) was dissolved in glacial acetic acid (6 ml). Iron powder (30 mg, 0.54 mmol) was added followed by a solution of bromine (0.36 ml) in glacial acetic acid (3 ml) slowly over 5 minutes. The resulting solution was stirred at 60° C. for 1 hour. A solution of bromine (0.13 ml) in glacial acetic acid (1 ml) was added and stirring was continued at 60° C. for 1.5 hours. The solution was allowed to cool to ambient temperature, diluted with water (20 ml). Excess bromine was destroyed by adding in sold sodium bisulphite until all the colour had disappeared. Solid sodium carbonate was added until the solution was basic and the resulting solution was then extracted with ethyl acetate (2×30 ml) and dried over sodium sulphate. Removal of the solvent gave an oil which was chromatographed on silica gel in diethyl ether giving the title compound as a clear oil (0.77 g, 54%). 1H NMR (250 MHz, CDCl3) δ 8.66-8.62 (2H, d, J=8.6 Hz), 7.87-7.86 (1H, d, J=2.2 Hz), 7.61-7.56 (1H, dd, J=8.5 Hz and 2.2 Hz), 7.48-7.46 (1H, d, J=8.5 Hz), 7.03-6.99 (2H, d, J=8.6 Hz), and 3.96 (3H, s). m/z (ES+) 264, 266 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06060469
출처 데이터셋uspto-grants-2000_05
ORD IDord-c0291c66fe7945558e0d4f5c91b4d080
출처 메모uspto-grants-2000_05