HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzenesulfonyl chloride → 5-Fluoro-1-(phenylsulfonyl)-1H-indole
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzenesulfonyl chloride | HCID 7369 | — |
| Edukt | 5-Fluoroindole | HCID 67861 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 5-Fluoro-1-(phenylsulfonyl)-1H-indole | HCID 11288858 | 74% |
Reaktionsschritte
KHMDS (0.5 M in toluene, 23 mL, 11.65 mmol) was added at 0° C. to a solution of 5-fluoroindole (1.5 g, 11.09 mmol) in DMF (23 mL). After stirring for 10 minutes, benzenesulfonyl chloride (1.55 mL, 12.209 mmol) was added. The ice-bath was removed and the mixture was stirred at room temperature for 4 hours. A saturated solution of NH4Cl was added to the reaction, and the resulting mixture was extracted with EtOAc. The combined organic extracts were washed with water and brine; dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was recrystallized from toluene to afford 2.26 g (74% yield) of 1-benzenesulfonyl-5-fluoro-1H-indole as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07776910B2 |
| Quelldatensatz | uspto-grants-2010_08 |
| ORD ID | ord-fdc0db041e3c4731bbd8402309b37211 |
| Quellennotiz | uspto-grants-2010_08 |