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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1439966생성일: 2026년 10월 27일

Dimethylformamide → (S)-Benzyl (2-oxotetrahydrofuran-3-yl)carbamate

https://huagongshe.com/reaction/1439966

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Cbz-L-HomoserineHCID 489187—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매WaterHCID 962—
생성물(S)-Benzyl (2-oxotetrahydrofuran-3-yl)carbamateHCID 48918584.3%

반응 단계

A mixture of N-benzyloxycarbonyl-(L)-homoserine (9.0 g), 1-hydroxybenzotriazole (HOBt) (5.4 g) and N,N-dimethylformamide (DMF) (50 ml) was provided and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSCD.HCl) (7.5 g) was added to the mixture under ice-cooling. The whole mixture was stirred at room temperature for 14 hours. The reaction mixture was then poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with 1% aqueous citric acid, water, saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride in the order mentioned and dried over MgSO4 and the solvent was distilled off, whereby (S)-3-(N-benzyloxycarbonylamino)tetrahydrofuran-2-one (7.0 g, 84.3%) was obtained. This product was recrystallized from dichloromethane-isopropyl ether. Colorless needles, m.p. 129°-130° C. Optical rotation [α]D -0.5° (C=0.52, CHCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05496834
출처 데이터셋uspto-grants-1996_03
ORD IDord-5eeee8c67d45497a852fd5dd5cfbdfa2
출처 메모uspto-grants-1996_03