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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1049589생성일: 2026년 10월 27일

Imidazole → 4-((Tert-butyl(dimethyl)silyl)oxy)-2'-fluoro-5'-methoxybiphenyl-2-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/1049589

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Ammonium ChlorideHCID 25517—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물2'-Fluoro-4-hydroxy-5'-methoxybiphenyl-2-yl trifluoromethanesulfonateHCID 117760123—
용매DimethylformamideHCID 6228—
생성물4-((Tert-butyl(dimethyl)silyl)oxy)-2'-fluoro-5'-methoxybiphenyl-2-yl trifluoromethanesulfonateHCID 13173603380%

반응 단계

To a solution of 2′-fluoro-4-hydroxy-5′-methoxybiphenyl-2-yl trifluoromethanesulfonate (2.85 g) and imidazole (800 mg) in DMF (50 mL) was added tert-butyldimethylchlorosilane (1.42 g), and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.99 g) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09382188B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-ccb2a4191dca44699145a6059d3a0472
출처 메모uspto-grants-2016_07