Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → (S)-Ethyl 2-((tert-butoxycarbonyl)amino)-3-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)propanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 반응물 | Ethyl N-(tert-butoxycarbonyl)-L-tyrosinate | HCID 11077750 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (S)-Ethyl 2-((tert-butoxycarbonyl)amino)-3-(4-(((trifluoromethyl)sulfonyl)oxy)phenyl)propanoate | HCID 10789275 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07476758B2 |
| 출처 데이터셋 | uspto-grants-2009_01 |
| ORD ID | ord-3e850b3097f0464d998f31c34c3981e3 |
| 출처 메모 | uspto-grants-2009_01 |