HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
O-Xylene → 4,8-Bis(trifluoromethyl)-10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | O-Xylene | HCID 7237 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-(2-Amino-4-trifluoromethylphenylthio)-3-trifluoromethylbenzonitrile | HCID 19969436 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Produkt | 4,8-Bis(trifluoromethyl)-10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-one | HCID 19969457 | — |
Reaktionsschritte
2-(2-Amino-4-trifluoromethylphenylthio)-3-trifluoromethylbenzonitrile (5.43 g, 15 mmol) was dissolved in a mixture of glacial acetic acid (60 ml), concentrated sulphuric acid (55 ml) and water (60 ml) and then heated under reflux for 8 hours. The cooled mixture was added to ice water (500 ml) and brought to pH 4 by addition of 10N aqueous sodium hydroxide. Extraction with dichloromethane followed by filtration, drying (sodium sulphate) and evaporation of the organic layer afforded a residue which was put into xylene (500 ml) and refluxed for 72 hours with azeotropic removal of water. The resulting solution was evaporated and the residue was recrystallised twice from ethanol to give the product as colourless needles (4.30 g, m/s, M+ =363).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05607929 |
| Quelldatensatz | uspto-grants-1997_03 |
| ORD ID | ord-17e84a3c41ea44e3a4633a93a698b915 |
| Quellennotiz | uspto-grants-1997_03 |