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HRID 376403作成日:2026年10月25日

Dibenzofuran → (S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acid

https://huagongshe.com/reaction/376403

反応式

関与物質

役割名称HCID仕込み量
反応物DibenzofuranHCID 568—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物(S)-(-)-2-(Trifluoroacetamido)succinic anhydrideHCID 12197622—
溶媒DichloromethaneHCID 6344—
生成物(S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acidHCID 5413194448%

反応手順

To a dichloromethane (50 mL) suspension of aluminum chloride (3.19 g, 0.024 mol) at 0° C., under an inert nitrogen atmosphere was added via a solid addition funnel an intimate mixture of N-trifluoroacetyl-L-aspartic acid anhydride (3.01 g, 0.0142 mol) and dibenzofuran (2 g, 0.0119 mol). The resulting brick-red suspension was allowed to warm to room temperature over 12 hours. The reaction mixture was poured into ice water (250 mL), and the resulting colorless biphasic mixture was extracted with ethyl acetate (4×100 mL). The combined organic extracts were washed with water (2×100 mL), brine (2×100 mL) and dried over magnesium sulfate. The mixture was filtered, and the organic solution was concentrated by evaporation of the solvent in vacuo to yield a white solid. The solid was recrystallized from 10% ethyl acetate/hexane (v/v) to give (S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acid (2.16 g, 48%) as a while solid; mp 174-176° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06020366
出典データセットuspto-grants-2000_02
ORD IDord-36d7ccd7f5ce4ca6b2b4f941420f8764
出典メモuspto-grants-2000_02