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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343890Erstellt: 25. Oktober 2026

Hydrochloric Acid → N-(2-amino-5-fluorobenzoyl)-8-aminocaprylic acid

https://huagongshe.com/reaction/343890

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
Edukt8-Aminooctanoic acidHCID 66085—
Edukt5-Fluoroisatoic anhydrideHCID 288560—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(2-amino-5-fluorobenzoyl)-8-aminocaprylic acidHCID 54514696—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A 50% (by weight) solution of potassium carbonate (11.2 mL, 16.8 mmol, 1.02 eq), 8-aminocaprylic acid (9.5 g, 59.7 mmol, 1.00 eq), 5-fluoroisatoic anhydride (10.82 g, 59.7 mmol, 1.00 eq), dioxane (40 mL), and water (5 mL) were added to a 100 mL round bottom flask equipped with a magnetic stir bar and a condenser. The red cloudy mixture was heated to 90° C. for 2 hours (at which time the reaction was determined, by HPLC, to have finished). The deep purple solution was cooled to 25° C. and acidified to pH=4.0 with 3% (by vol.) aqueous hydrochloric acid. The dark precipitate which formed was isolated by filtration. The solid was recrystallized from 50 mL of 65% ethanol-water, recovered by filtration, and dried over 6 hours in a 50° C. vacuum oven. The N-(2-amino-5-fluorobenzoyl) -8-aminocaprylic acid was isolated as a light yellow solid (11.86 g, 67%), mp=108°-109° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05863944
Quelldatensatzuspto-grants-1999_01
ORD IDord-7f10fbb58d0f47db819aaa186b5b9ccd
Quellennotizuspto-grants-1999_01