HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 885912Erstellt: 26. Oktober 2026
Iodine → Benzenesulfonamide, 4-amino-3-iodo-N,N-dimethyl-
https://huagongshe.com/reaction/885912
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Benzenesulfonamide, 4-amino-N,N-dimethyl- | HCID 74369 | — |
| Katalysator | HCID 178418844 | HCID 178418844 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Benzenesulfonamide, 4-amino-3-iodo-N,N-dimethyl- | HCID 21906367 | 165,9% |
Reaktionsschritte
To a stirred solution of 4-amino-N,N-dimethylbenzenesulfonamide (3.0 g, 14.98 mmol) in EtOH (165 mL) at 50° C. was added a slurry of iodine (1.3 g, 4.99 mmol) and silver sulfate (2.8 g, 9.00 mmol) in EtOH (40 mL). The same addition was repeated after 1 h of stirring at 50° C., then the reaction mixture was stirred at 50° C. for 16 h. Iodine (0.76 g, 3.00 mmol) was again added, and the mixture stirred at 50° C. for 2 h before being filtered through Celite®. The filtrate was concentrated in vacuo, and EtOH (70 mL) was added. The suspension was stirred at 50° C. for 1 h, cooled to r.t., then filtered to give the title compound (2.7 g, 55%) as a brown solid that was used without further purification. δH (DMSO-d6) 7.81 (1H, d, J 2.1 Hz), 7.42 (1H, dd, J 8.6 and 2.1 Hz), 6.83 (1H, d, J 8.6 Hz), 6.12 (2H, br. s), 2.58 (6H, s). LCMS (ES+) 326.9 (M+H)+, RT 2.50 minutes (Method 3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08242116B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-8c6efc0a8e54436eaf6468697e075fea |
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| Quellennotiz | uspto-grants-2012_08 |
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