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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1626717생성일: 2026년 10월 27일

Diethyl Ether → trifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl ester

https://huagongshe.com/reaction/1626717

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물Trifluoro-methanesulfonic acid 2-hydroxy-3-(3-morpholin-4-yl-3-oxo-propionyl)-phenyl esterHCID 11610960—
용매DichloromethaneHCID 6344—
생성물trifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl esterHCID 11603298—

반응 단계

Trifluoro-methanesulfonic acid 2-hydroxy-3-(3-morpholin-4-yl-3-oxo-propionyl)-phenyl ester [D] (1.06 g, 2.7 mmol) in dichloromethane (30 ml) was treated with trifluoromethanesulphonic anhydride and stirred over night at room temperature. The reaction mixture was then concentrated, re-dissolved in methanol and stirred for a further 2 hours. The solution was diluted with water and basified to pH8. It was then extracted three times with dichloromethane. The extracts were combined, washed with brine, dried with magnesium sulphate and evaporated to give the crude product as a brown oil. Trituration with ether gave trifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl ester [E] as a brown solid. Yield 210 mg, 20%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785457B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-69c6190df50d495ab6df064ab3ab381b
출처 메모uspto-grants-2014_07