HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Iodine → 4-Chloro-6-fluoro-2-(4-fluorophenyl)quinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Chloro-6-fluoroquinoline | HCID 2736586 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 4-Chloro-6-fluoro-2-(4-fluorophenyl)quinoline | HCID 13603897 | 50,8% |
Reaktionsschritte
To a solution of 4.37 g (25 mmol) of 1-bromo-4-fluorobenzene in 35 ml of ether cooled to -10° was added 15 ml of a 1.6M solution of butyl lithium in hexane in portions while maintaining the temperature below 0°. This mixture was stirred below 0° for 15 min. A solution of 3.63 g (20 mmol) of 4-chloro-6-fluoroquinoline in 20 ml of tetrahydrofuran was added while maintaining the temperature below 0°. The dark solution was stirred at room temperature for 20 min. To the reaction mixture was then added 5 ml of water and 5 g of iodine, and 10 ml of 3N sodium hydroxide. After 10 min of stirring the solid was collected to give 2.8 g of product, mp 130°-133°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04560692 |
| Quelldatensatz | uspto-grants-1985_12 |
| ORD ID | ord-5ff4f36850a84cac9655db6ac5e43a06 |
| Quellennotiz | uspto-grants-1985_12 |