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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247839생성일: 2026년 10월 24일

Trifluoromethanesulfonic acid → N-[2-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-propenyl-L-serine, methyl ester

https://huagongshe.com/ko/reaction/247839

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물Allyl 2,2,2-TrichloroacetimidateHCID 316905—
반응물N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-L-serine, methyl esterHCID 67799768—
용매DichloromethaneHCID 6344—
용매Dichloromethane cyclohexaneHCID 21916607—
생성물N-[2-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-O-2-propenyl-L-serine, methyl esterHCID 70044917—

반응 단계

Dissolve N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-L-serine, methyl ester (25 g, 63 mmol) in methylene chloride/cyclohexane (1:1, 600 mL). Add allyl trichloroacetimidate (26 g, 128 mmol) and trifluoromethanesulfonic acid (5 mL), 56.6 mmol). Stir at room temperature under a nitrogen atmosphere for 5 hours and dilute with methylene chloride. Wash with saturated aqueous sodium hydrogen carbonate, water, dry (MgSO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography (gradient 20% ethyl acetate/hexane to 35% ethyl acetate/hexane) to give the title compound; mp 95°-97° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05208230
출처 데이터셋uspto-grants-1993_05
ORD IDord-ea165866ae234749973fbe2e4a3ff052
출처 메모uspto-grants-1993_05