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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1626716생성일: 2026년 10월 27일

Hydrochloric Acid → Trifluoro-methanesulfonic acid 2-hydroxy-3-(3-morpholin-4-yl-3-oxo-propionyl)-phenyl ester

https://huagongshe.com/reaction/1626716

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-AcetylmorpholineHCID 15543—
반응물Lithium diisopropylamideHCID 2724682—
반응물Methyl 2-hydroxy-3-(trifluoromethylsulfonyloxy)benzoateHCID 11616395—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Trifluoro-methanesulfonic acid 2-hydroxy-3-(3-morpholin-4-yl-3-oxo-propionyl)-phenyl esterHCID 11610960—

반응 단계

A solution of N-acetylmorpholine (1.72 g, 13.3 mmol, 2 eq) in 30 ml dry tetrahydrofuran under nitrogen was cooled in an acetone/dry ice bath (−78° C.) and treated with LDA (10 ml, 2M solution in THF, 3 eq). The reaction mixture was stirred for 60 minutes then 2-hydroxy-3-trifluoromethanesulfonyloxy-benzoic acid methyl ester [α] (2 g, 6.6 mmol, 1 eq as a solution in 10 ml dry THF) was added. The reaction mixture was allowed to warm from −78° C. to room temperature and stirred over night. The reaction was diluted with water (4 ml) followed by 2M hydrochloric acid (40 ml), then extracted three times with dichloromethane. The extracts were combined, washed with brine, dried with magnesium sulphate, filtered and evaporated. The crude product was purified by flash chromatography eluting with ethyl acetate to afford trifluoro-methanesulfonic acid 2-hydroxy-3-(3-morpholin-4-yl-3-oxo-propionyl)-phenyl ester [D]. Yield 1.06 g, 40%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785457B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-a2acae143ffc4ae8b9c53dd95ce7d47c
출처 메모uspto-grants-2014_07