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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2043293생성일: 2026년 10월 25일

Potassium Iodide → 4-[5,6-Dichloro-2-(2,2,2-trifluoro-ethyl)-benzoimidazol-1-ylmethyl]-benzoic acid ethyl ester

https://huagongshe.com/reaction/2043293

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 4-(bromomethyl)benzoateHCID 954261—
반응물5,6-Dichloro-2-(2,2,2-trifluoro-ethyl)-1H-indoleHCID 66968833—
반응물dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzoimidazoleHCID 66968977—
용매DimethylformamideHCID 6228—
생성물4-[5,6-Dichloro-2-(2,2,2-trifluoro-ethyl)-benzoimidazol-1-ylmethyl]-benzoic acid ethyl esterHCID 44430201—

반응 조건

온도0 °C

반응 단계

NaH (60%) 120 mg, 3 mmol) was added into a solution of dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzoimidazole. 5,6-Dichloro-2-(2,2,2-trifluoro-ethyl)-1H-indole (538 mg, 2 mmol) in DMF (5 ml) at 0° C. The resulting mixture was stirred at 0° C. for half hour. Ethyl 4-(bromomethyl)-benzoate (729.3 mg, 3 mmol) and potassium iodide (498 mg, 3 mmol) were then added to the reaction mixture at 0° C. The reaction temperature was raised to 25° C. and then the reaction mixture was stirred for 18 hours. NH4Cl (aq.) was added and extracted with EtOAc. The organic layer was washed with brine, then dried over anhydrous MgSO4. The solvent was distilled out under reduced pressure. Column chromatography (silica gel, EtOAc/hexanes (0% to 60%) yielded the title compound as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08586616B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-e288c591cd2140dbb1551511797168ce
출처 메모uspto-grants-2013_11