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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 897471생성일: 2026년 10월 25일

Water → 2-(4-Iodophenoxy)pyrimidine

https://huagongshe.com/reaction/897471

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-IodosuccinimideHCID 120273—
반응물2-PhenoxypyrimidineHCID 5324768—
용매Trifluoroacetic acidHCID 6422—
용매Trifluoroacetic anhydrideHCID 9845—
생성물2-(4-Iodophenoxy)pyrimidineHCID 148461750%

반응 단계

A mixture of 2-phenoxypyrimidine (int AY) (4.03 g, 0.0234 mol) and N-iodosuccinimide (10.52 g, 0.0468 mol) in trifluoroacetic acid (40 mL) and trifluoroacetic anhydride (8 mL) was heated at reflux for 4 hours. The mixture was allowed to cool to ambient temperature and water (75 mL) was added. The mixture was extracted with three times with 50 mL. The combined organic layers were washed twice with saturated aqueous sodium bicarbonate (50 mL), twice with 10% aqueous sodium thiosulfate (50 mL) and brine (50 mL). The organic layer was dried over magnesium sulfate, filtered and the solvent was removed in vacuo. The crude solid was purified by flash column chromatography on silica gel using n-heptane/ethyl acetate (3:1) as an eluent to give 2-(4-iodophenoxy)pyrimidine as a light yellow solid (3.49 g, 0.0117 mol): 1H NMR (CDCl3, 400 MHz) 8.57 (d, 2H), 7.73 (d, 2H), 7.07 (t, 1H), 6.98 (d 2H); TLC (n-heptane/ethyl acetate=1:1) Rf 0.45.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06921763B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-d901760092454903a32d8b8b602290fa
출처 메모uspto-grants-2005_07