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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366315생성일: 2026년 10월 26일

Water → 3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-1-methyl-6-trifluoromethyluracil

https://huagongshe.com/reaction/366315

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-6-trifluoromethyluracilHCID 23289176—
용매DimethylformamideHCID 6228—
생성물3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-1-methyl-6-trifluoromethyluracilHCID 1547720894.5%

반응 단계

0.50 g (1.3 mmol) of 3-(4-chloro-2-ethyl-6-fluorobenzofuran-7-yl)-6-trifluoromethyluracil and 0.30 g (2.3 mmol) of potassium carbonate, were suspended in 20 ml of N,N-dimethylformamide, and 0.23 g (1.6 mmol) of methyl iodide was dropwise added thereto under cooling with ice. After stirring at room temperature for 3 hours, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed sequentially with water and a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Then, the obtained residue was purified by silica gel column chromatography to obtain 0.48 g (yield: 92%) of the desired product as white crystals. Melting point: 142-143° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06130187
출처 데이터셋uspto-grants-2000_10
ORD IDord-4cc8c6405c384e7bae5f92be5d72802b
출처 메모uspto-grants-2000_10