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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 368931Erstellt: 24. Oktober 2026

Triethylamine → (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid

https://huagongshe.com/de/reaction/368931

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAcetic acid, 2-fluoro-, 1,1'-anhydrideHCID 67886—
EduktN-(tert-butoxycarbonyl)-L-aspartic acidHCID 99718—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelBenzeneHCID 241—
Produkt(S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acidHCID 10131156—

Reaktionsschritte

A suspension of Boc-Asp-OH (8.11 mmol) and fluoroacetic anhydride (16.2 mmol) in benzene (30 ml) was treated with triethylamine (16.2 mmol) at room temperature. The catalyst 4-dimethylaminopyridine (0.41 mmol) was added to the solution and the reaction stirred for about 2 h at room temperature. About 100 ml benzene was added to the reaction mixture. The organic solution was washed with 1N HCl (2×50 ml), saturated NaHCO3 (2×50 ml), and saturated NaCl (2×50 ml), followed by drying over anhydrous MgSO4. The solvent was then removed by evaporation under reduced pressure. The resulting oil was applied to a 2.5×80 cm column of silica gel (60-200 mesh). The title compound was eluded with 2% methanol in chloroform.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06136787
Quelldatensatzuspto-grants-2000_10
ORD IDord-d404ed8a393943249af15d1d9d99dbdc
Quellennotizuspto-grants-2000_10