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HRID 62435作成日:2026年10月26日

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

https://huagongshe.com/reaction/62435

反応式

関与物質

役割名称HCID仕込み量
反応物L-HomoserineHCID 12647—
反応物N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
反応物Sodium BicarbonateHCID 516892—
反応物Diethylether waterHCID 21584184—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物(2S)-2-(((9H-fluoren-9-ylmethoxy)carbonyl)amino)-4-hydroxybutanoic acidHCID 1544997188%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09446157B2
出典データセットuspto-grants-2016_09
ORD IDord-13d45cf8286f4c1b922e0a1388f241ba
出典メモuspto-grants-2016_09