戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1489513作成日:2026年10月25日

Hydrochloric Acid → Fmoc-L-aspartic acid

https://huagongshe.com/reaction/1489513

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物L-Aspartic AcidHCID 5960—
反応物Sodium CarbonateHCID 10340—
反応物N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物Fmoc-L-aspartic acidHCID 701901671%

反応手順

Forty-five g (0.134M, 0.96 eq) of Fmoc-Osu was added to 20 g (0.15M, 1 eq) of aspartic acid and 20 g of Na2CO3 dissolved in 400 mL of water and 200 mL of dioxane. The mixture was stirred for 2 hrs while the pH was maintained at about 9 by the addition of small amounts of Na2 CO3. Then the cloudy white mixture was poured into 500 mL of ice water containing 40 mL of conc HCl. The white solid was extracted with 500 mL EtOAc and this was mixed with 500 mL of hexane. The mixture was chilled overnight and stirred the next day to give 38 g of Fmoc-aspartic acid as crystals (71% yield) upon filtration and air drying. 10 g (0.28M) of this product was dissolved in 200 mL of methanol and 20 mL of conc H2 SO4 was added. The solution was allowed to stand overnight. The mixture was poured into 1 L of water and filtered. The resulting white solid was dried and redissolved in EtOAc. Slow addition of hexane and chilling gave 9 g (83% yield) of product as white needles, mp 78°-80°. [a]d =-13.9°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05679643
出典データセットuspto-grants-1997_10
ORD IDord-c8f32a38fe304c6ab3cff99b00cc479b
出典メモuspto-grants-1997_10