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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432175생성일: 2026년 10월 27일

Water → 5-Bromo-2-phenoxypyrimidine

https://huagongshe.com/reaction/432175

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PhenolHCID 996—
반응물Potassium HydroxideHCID 14797—
반응물5-Bromo-2-chloropyrimidineHCID 606665—
촉매Dibenzo-18-crown-6HCID 26541—
용매TolueneHCID 1140—
생성물5-Bromo-2-phenoxypyrimidineHCID 64284254.4%

반응 단계

A mixture of 5-bromo-2-chloropyrimidine (5.00 g, 0.0259 mol), phenol (3.16 g, 0.0336 mol), dibenzo-18-crown-6 (0.47 g, 0.0013 mol) and ground potassium hydroxide (3.51 g, 0.0626 mol) in toluene (75 ml) was heated at reflux for 5 hours with azeotropic removal of water. The mixture was allowed to cool to ambient temperature and the solvent was removed under reduced pressure. The residue was partitioned between water and chloroform. The layers were separated and the aqueous phase was extracted with chloroform three times. The combined organic layers were dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography on silica using n-heptane/ethyl acetate (98:2) as an eluent to give 5-bromo-2-phenoxy-pyrimidine as a white solid (3.55 g, 0.0141 mol): 1H NMR (DMSO-d6, 400 MHz) 8.80 (s, 2H), 7.45 (t, 2H), 7.27 (t, 1H), 7.22 (d 2H); TLC (n-heptane/ethyl acetate=95:5) Rf 0.20.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660744B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-1bbc8bd3d0a34185a80347e464788c0c
출처 메모uspto-grants-2003_12