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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15899Erstellt: 23. Oktober 2026

Allyl Alcohol → N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamide

https://huagongshe.com/de/reaction/15899

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl AlcoholHCID 7858—
EduktSodium BicarbonateHCID 516892—
EduktN-(3-iodophenyl)methanesulfonamideHCID 21830928—
KatalysatorPalladium ChlorideHCID 24290—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamideHCID 5744437360,5%

Reaktionsschritte

A mixture of N-(3-iodo-phenyl)-methanesulfonamide (2.4 g, 8 mmol), tetra-n-butyl-ammonium chloride (2.22 g, 8 mmol), allyl alcohol (0.7 g, 12 mmol), sodium hydrogencarbonate (1.6 g, 19 mmol) and palladium(II) chloride (0.36 g, 1.8 mmol) in anhydrous dimethylformamide (30 mL) was stirred at room temperature for 48 h under argon. The mixture was then diluted with 5% aqueous hydrochloric acid (100 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layers were dried (sodium sulfate) and evaporated in vacuo. The crude product was purified by silica gel chromatography (ethyl acetate in hexane, 30% to 50%) to give the title compound as an amber oil (1.1 g, 60%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732600B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-c3abfdc781784af8ae3f38b4d5d92de5
Quellennotizuspto-grants-2010_06