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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 376403Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/376403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibenzofuranHCID 568—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt(S)-(-)-2-(Trifluoroacetamido)succinic anhydrideHCID 12197622—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acidHCID 5413194448%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06020366
Quelldatensatzuspto-grants-2000_02
ORD IDord-36d7ccd7f5ce4ca6b2b4f941420f8764
Quellennotizuspto-grants-2000_02