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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 8-Aminooctanoic acid | HCID 66085 | — |
| Edukt | 5-Fluoroisatoic anhydride | HCID 288560 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | N-(2-amino-5-fluorobenzoyl)-8-aminocaprylic acid | HCID 54514696 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05863944 |
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| Quelldatensatz | uspto-grants-1999_01 |
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| ORD ID | ord-7f10fbb58d0f47db819aaa186b5b9ccd |
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| Quellennotiz | uspto-grants-1999_01 |
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