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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20522생성일: 2026년 10월 25일

Citric Acid → 3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)benzoic acid

https://huagongshe.com/reaction/20522

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Sodium BicarbonateHCID 516892—
반응물3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-[(1S)-2-hydroxy-1-methylethoxy]benzoic acidHCID 59346883—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)benzoic acidHCID 59346909—

반응 단계

A mixture of 3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-[(1S)-2-hydroxy-1-methylethoxy]benzoic acid (9.8 g, 0.025 mol), t-butyldimethylsilylchloride (11.3 g, 0.075 mol) and imidazole (17.08 g, 0.25 mol) in DMF (100 mL) was stirred at RT for 24 hours. Water (100 mL) was added and the mixture extracted into diethyl ether (3×100 mL). The extracts were combined and washed with water (3×100 mL), brine (100 mL), dried (MgSO4), filtered, and evaporated in vacuo to give a golden oil. Saturated aqueous sodium bicarbonate (100 mL) and diethyl ether (100 mL) were added and stirred for 30 mins. The aqueous layer was acidified with 1M citric acid solution and extracted into diethyl ether (3×100 mL). The extracts were combined, dried (MgSO4), filtered, and evaporated in vacuo and the crude product chromatographed on silica, eluting with ethyl acetate, to give the desired compound. (6.32 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745475B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-159f422bd884422f8a95d077a5d152fa
출처 메모uspto-grants-2010_06