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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10300Erstellt: 24. Oktober 2026

Acetic Acid → 2-Cyclopropylamino-4,5-difluorobenzoic acid

https://huagongshe.com/de/reaction/10300

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2-Amino-4,5-difluorobenzoic acidHCID 735965—
Edukt(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Cyclopropylamino-4,5-difluorobenzoic acidHCID 1499747394,8%

Reaktionsschritte

To a solution of 4,5-difluoroanthranilic acid (1.13 g, 6.53 mmol) in anhydrous methanol (40 mL) is added molecular sieves (3 Å), acetic acid (3.70 mL, 65.3 mmol) and [(1-ethoxycyclopropyl)oxy]trimethylsilane (5.25 mL, 26.11 mmol). After 30 minutes, sodium cyanoborohydride (2.08 g, 32.64 mmol) is added, and the reaction mixture is heated to reflux. After 16 hours, the reaction is cooled to room temperature, filtered, washed with methanol, and the combined filtrate concentrated under vacuum to afford a viscous oil. The resulting oil is dissolved in ethyl acetate and washed with 1.0 M hydrochloric acid, water, and brine. The organic layer is dried over MgSO4, filtered, and the filtrate is concentrated under vacuum to afford as a beige solid (1.32 g). MS CI: m/z 212 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094780B1
Quelldatensatzuspto-grants-2006_08
ORD IDord-c17e0a2a9f6b4b76a94d85708a9a1372
Quellennotizuspto-grants-2006_08