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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 2-Amino-4,5-difluorobenzoic acid | HCID 735965 | — |
| Edukt | (1-Ethoxycyclopropoxy)trimethylsilane | HCID 2734686 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Cyclopropylamino-4,5-difluorobenzoic acid | HCID 14997473 | 94,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07094780B1 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-c17e0a2a9f6b4b76a94d85708a9a1372 |
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| Quellennotiz | uspto-grants-2006_08 |
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