HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072607Erstellt: 23. Oktober 2026
Dichloromethane → 5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole
https://huagongshe.com/de/reaction/1072607
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Benzenesulfonyl chloride | HCID 7369 | — |
| Edukt | Iodine chloride | HCID 24640 | — |
| Edukt | 5,7-difluoro-1H-indole | HCID 2778730 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | 5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole | HCID 22014784 | 87% |
Reaktionsschritte
The 1.0 M ICl in CH2Cl2 (43 ml, 43 mmol) is added to a solution of 5,7-difluoro-indole (6 g, 39 mmol) in 35 ml pyridine under N2 at 0° C. and the resulting mixture is stirred for 30 minutes. The reaction is diluted with toluene and washed with brine, 1N HCl, 1N NaOH, dried (Na2SO4), filtered and concentrated. The crude 3-iodo-5,7-difluoroindole is stirred in toluene (85 ml) and 5 N NaOH (70 ml), tetrabutylammonium bromide (1.25 g, 3.9 mmol), then benzenesulfonyl chloride (6.2 ml, 48 mmol) are added and the resulting mixture is stirred 24 hours. The two phase reaction mixture is diluted with toluene, washed with brine, dried(Na2SO4), filtered, concentrated and the residue is triturated with diethyl ether/petroleum ether. The resulting solid is filtered to give 14.2 g of N-Benzenesulfonyl-3-iodo-5,7-difluoroindole (87%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06911463B2 |
|---|
| Quelldatensatz | uspto-grants-2005_06 |
|---|
| ORD ID | ord-c496902e20ac473d8baa4a21b4e14b25 |
|---|
| Quellennotiz | uspto-grants-2005_06 |
|---|