HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
p-Aminoacetophenone → N-(4-acetylphenyl)methanesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | p-Aminoacetophenone | HCID 7468 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | N-(4-acetylphenyl)methanesulfonamide | HCID 684083 | 95% |
Reaktionsschritte
A cooled solution of 4′-aminoacetophenon (10 mmol) in pyridine (10 mL) at 0° C. was treated with methanesulfonyl chloride (15 mmol) and stirred at room temperature for 2 h. The reaction mixture was diluted with H2O and extracted with EtOAc several times. The combined organic layers were washed with H2O and brine, dried over MgSO4, filtered, and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes to afford 4′-(Methylsulfonylamino)acetophenone (13-5, LJO-298).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08642657B2 |
| Quelldatensatz | uspto-grants-2014_02 |
| ORD ID | ord-ce529ee51da142f182b51d887ecae8d4 |
| Quellennotiz | uspto-grants-2014_02 |