Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Cinnamic Acid | HCID 444539 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Cinnamoyl Chloride | HCID 5354261 | 135,9% |
Reaktionsschritte
trans-Cinnamic acid (5 g, 33.7 mmol, Aldrich) was dissolved in toluene (100 mL), and the solution was cooled to 0° C. and flushed with N2. Anhydrous DMF (0.1 mL) was added, followed by oxalyl chloride (8.56 g, 5.88 mL, 67.4 mmol) dropwise over 8 minutes. The mixture was stirred at 0° C. for 1 hour and at room temperature for 1.5 hours. The solvent was removed under vacuum to give the title compound (7.63 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05618949 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-5922897b2fd84ef282b4a00b663a2f4c |
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| Quellennotiz | uspto-grants-1997_04 |
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