HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238932Erstellt: 24. Oktober 2026
Hydrochloric Acid → N-(4-Acetyl-2-fluorophenyl)methanesulfonamide
https://huagongshe.com/de/reaction/238932
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Butyl vinyl ether | HCID 8108 | — |
| Edukt | thallium(I) acetate | HCID 11247 | — |
| Edukt | N-(2-Fluoro-4-iodophenyl)methanesulfonamide | HCID 19785608 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | N-(4-Acetyl-2-fluorophenyl)methanesulfonamide | HCID 58755745 | — |
Reaktionsschritte
A mixture of N-(2-Fluoro-4-iodophenyl)methanesulfonamide (13-3, 5 mmol) and palladium(II)acetate (0.15 nM, 0.034 g), 1,3-bisdiphenyl phosphinoprophan (0.3 mM, 0.124 g), thallium(I)acetate (5.5 mM, 1.450 g) and butylvinyl ether (10 mM, 1.3 mL) in DMF (10 mL) was heated at 95° C. for 19 h. The reaction mixture was cooled to room temperature, diluted with THF, treated with 10% HCl (10 mL) and stirred at room temperature. A mixture was diluted with EtOAc, washed with ammonium chloride solution three times and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes as eluant to 3′-Fluoro-4′-(methylsulfonylamino)acetophenone (13-6, LJO-363).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08642657B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-1e154d2223aa4f1f859ba08d87aad887 |
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| Quellennotiz | uspto-grants-2014_02 |
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