Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Nitro-2,5-xylidine | HCID 18963 | — |
| Edukt | 4-Methoxybutan-2-one-dimethylacetal | HCID 81084 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4,5,8-Trimethyl-6-nitroquinoline | HCID 10560662 | — |
Reaktionsschritte
A mixture of 2,5-dimethyl-4-nitroaniline (0.96 g), ferric chloride hexahydrate (2.50 g), zinc chloride (0.094 g), concentrated hydrochloric acid (0.481 mL), and ethanol (8 mL) is heated to 60° C. 1,3,3-trimethoxybutane (0.73 mL) is added dropwise while the reaction mixture is kept at 60° C. The reaction mixture is heated at reflux overnight and cooled to room temperature. A solution of 10% aqueous sodium hydroxide is added, and the mixture is extracted three times with methylene chloride. The combined organic layers are dried over sodium sulfate, filtered and evaporated to afford a crude product. The crude product is purified by flash chromatography using 25% ethyl acetate in hexane as eluent, providing 6-nitro-4,5,8-trimethylquinoline.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05578607 |
|---|
| Quelldatensatz | uspto-grants-1996_11 |
|---|
| ORD ID | ord-f54c31b105564ebf9ec27a26c5c28f03 |
|---|
| Quellennotiz | uspto-grants-1996_11 |
|---|