HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Toluene → 1-(4-Chlorobenzenesulfonyl)-5-fluoro-1H-indole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 5-Fluoroindole | HCID 67861 | — |
| Katalysator | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(4-Chlorobenzenesulfonyl)-5-fluoro-1H-indole | HCID 22220126 | 75,9% |
Reaktionsschritte
A mixture of 5-fluoroindole (1.0 g, 7.4 mmole), 4-chlorobenzenesulfonyl chloride (1.6 g, 7.6 mmole), tetra-n-butylammonium hydrogen sulfate (0.05 g), 4N sodium hydroxide (5 mL, 20 mmol), and toluene (6 mL) was stirred at room temperature for 15 h. The mixture was diluted with 10 mL water and extracted with 25 mL ethyl acetate. The organic phase was washed with 10 mL water, 10 mL saturated sodium chloride, and then dried (anhydrous magnesium sulfate). The solution was concentrated under reduced pressure. The residue was recrystallized from ethyl ether/hexane to provide 1-(4-Chlorobenzenesulfonyl)-5-fluoro-1H-indole (1.74 g) m.p. 108–109°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07022708B2 |
| Quelldatensatz | uspto-grants-2006_04 |
| ORD ID | ord-616b2c0f6a604a29b66a75f3e1e10247 |
| Quellennotiz | uspto-grants-2006_04 |