HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2361610Erstellt: 26. Oktober 2026
Triethylamine → (E)-3-(4-fluorophenyl)acryloyl azide
https://huagongshe.com/reaction/2361610
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Edukt | 4-Fluorocinnamic acid | HCID 1530234 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | (E)-3-(4-fluorophenyl)acryloyl azide | HCID 86683266 | 90,7% |
Reaktionsschritte
To a solution of (E)-3-(4-fluorophenyl)acrylic acid (25 g, 150 mmol) in benzene (120 mL) was added triethylamine (30.5 g, 301 mmol) followed by DPPA (41.4 g, 150 mmol) at room temperature. The reaction mass was stirred at the same temperature for 18 h. The solvent was evaporated under reduced pressure and the residue was diluted with water and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to get crude compound. The crude compound was purified by conventional column chromatography (Silica gel, 60-120 mesh) using 10% ethyl acetate in pet ether as mobile phase to get the desired compound as a white solid (26 g, 90%). 1H NMR (400 MHz, CDCl3): δ ppm 7.73-7.69 (d, J=16 Hz, 1H), 7.55-7.51 (m, 2H), 7.11-7.07 (m, 2H), 6.36-6.32 (d, J=16 Hz, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08691757B2 |
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| Quelldatensatz | uspto-grants-2014_04 |
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| ORD ID | ord-96d31ba597a449f4b0d2b87a68965ea5 |
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| Quellennotiz | uspto-grants-2014_04 |
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