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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktButyl vinyl etherHCID 8108—
Eduktthallium(I) acetateHCID 11247—
EduktN-(2-Fluoro-4-iodophenyl)methanesulfonamideHCID 19785608—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(4-Acetyl-2-fluorophenyl)methanesulfonamideHCID 58755745—

Reaktionsbedingungen

Temperatur95 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642657B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-1e154d2223aa4f1f859ba08d87aad887
Quellennotizuspto-grants-2014_02