HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Chloro-7-(trifluoromethyl)quinoline → 4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Chloro-7-(trifluoromethyl)quinoline | HCID 67668 | — |
| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinoline | HCID 23128133 | — |
Reaktionsschritte
To 14 mL of a chloroform solution containing 0.90 g of 4-chloro-7-trifluoromethylquinoline, 1.04 g of m-chloroperbenzoic acid was added, and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with 15 mL of an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain a yellow solid, 4-chloro-7-trifluoromethylquinoline N-oxide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08524738B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-0c9d7f38499840a9bd74ad95e8a955b4 |
| Quellennotiz | uspto-grants-2013_09 |