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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62435생성일: 2026년 10월 26일

L-Homoserine → (2S)-2-(((9H-fluoren-9-ylmethoxy)carbonyl)amino)-4-hydroxybutanoic acid

https://huagongshe.com/reaction/62435

반응식

참여 물질

역할이름HCID투입량
반응물L-HomoserineHCID 12647—
반응물N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
반응물Sodium BicarbonateHCID 516892—
반응물Diethylether waterHCID 21584184—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물(2S)-2-(((9H-fluoren-9-ylmethoxy)carbonyl)amino)-4-hydroxybutanoic acidHCID 1544997188%

반응 단계

L-homoserine (15 g, MW119.12, 0.126 mol) and NaHCO3 (22 g, MW84, 0.26 mol) were dissolved in water (600 mL). The solution was chilled in an ice bath, followed by addition of Fmoc-OSu (42.5 g, MW337.3, 0.126 mol) in acetone (400 mL). The mixture was stirred overnight. A mixture of ether/water (200 mL/200 mL) was added, and the solid was filtered off. The filtrate was separated and the aqueous phase was washed with ethyl twice (100 mL×2), followed by acidifying with 3N HClaq (about 100 mL) to pH3-4. The suspension was extracted with ether (200 mL×2). The combined organic phases were washed with brine once (100 mL) and dried over Na2SO4. After evaporation, white solid was obtained (weight: 38 g, yield: 88%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09446157B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-13d45cf8286f4c1b922e0a1388f241ba
출처 메모uspto-grants-2016_09