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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1454107생성일: 2026년 10월 25일

Water → (S)-Ethyl 2-((tert-butoxycarbonyl)amino)-3-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)propanoate

https://huagongshe.com/reaction/1454107

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PyridineHCID 1049—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물Ethyl N-(tert-butoxycarbonyl)-L-tyrosinateHCID 11077750—
용매DichloromethaneHCID 6344—
생성물(S)-Ethyl 2-((tert-butoxycarbonyl)amino)-3-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)propanoateHCID 10789275100%

반응 단계

Under nitrogen atmosphere, pyridine(130.3 g) and trifluoromethanesulfonic anhydride (170.4 g) were added dropwise to a solution of ethyl (αS)-α-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybenzenepropionate (170.0 g) in dichloromethane (1.7 L) at 10° C. or below. After stirring for 1 hour at the same temperature, water (850 ml) was added dropwise to the mixture and the mixture was stirred for 2 hours at the same temperature. The organic layer was washed with 10% aqueous citric acid solution and aqueous saturated sodium hydrogen carbonate solution, and dried over magnesium sulfate. The solvent was removed in vacuo to yield ethyl (αS)-α-[[(1,1-dimethylethoxy)carbonyl]amino]-4-(trifluoromethanesulfonyloxy)benzenepropionate (242.5 g) as oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07476758B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-3e850b3097f0464d998f31c34c3981e3
출처 메모uspto-grants-2009_01