HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Carbon Dioxide → N-[4-(1,3-Dioxo-indan-2-yl)-phenyl]-acetamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Actarit | HCID 2018 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N-[4-(1,3-Dioxo-indan-2-yl)-phenyl]-acetamide | HCID 853463 | — |
Reaktionsbedingungen
| Temperatur | 70 °C |
|---|
Reaktionsschritte
A mixture of (4-acetylamino-phenyl)-acetic acid (15 g, Reference Example 15) phthallic anhydride (15.8 g) and triethylamine (42.3 mL) was heated at 70° C. for 3 minutes then treated with acetic anhydride (105.8 mL). The mixture was heated on a steam bath at approximately 70° C. until evolution of carbon dioxide ceased. The resulting deep red solution was evaporated and the residue was treated with water (750 mL) then heated on a steam bath for 2 hours. The insoluble material was filtered, dried under vacuum and then subjected to chromatography on silica eluting with mixtures of dichloromethane and methanol (99:5 to 50:50, v/v) to give the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07166616B2 |
| Quelldatensatz | uspto-grants-2007_01 |
| ORD ID | ord-0c976903602b4d9caa779e87566012c1 |
| Quellennotiz | uspto-grants-2007_01 |