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HRID 15857Erstellt: 23. Oktober 2026

N,N'-Dimethylethylenediamine → 3-[3-(2-Hydroxyethyl)phenyl]-1,3-oxazolidin-2-one

https://huagongshe.com/de/reaction/15857

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N'-DimethylethylenediamineHCID 8070—
EduktPotassium CarbonateHCID 11430—
EduktAmmonium ChlorideHCID 25517—
Edukt2-(3-Bromophenyl)ethan-1-olHCID 2734090—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-[3-(2-Hydroxyethyl)phenyl]-1,3-oxazolidin-2-oneHCID 5424381164%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A solution 2-(3-bromophenyl)ethanol (1.00 g, 5.00 mmol), 2-oxazolidin-2-one (874 mg, 10.04 mmol), copper(I)iodide (96 mg, 0.50 mmol), N,N′-dimethyl-1,2-ethanediamine (60 μL, 49 mg, 0.56 mmol) and potassium carbonate (1.04 g, 7.50 mmol) were suspended in dioxane (6 mL). The mixture was stirred under nitrogen for 2.5 h at 100° C. After addition of copper(I)iodide (96 mg, 0.50 mmol) and N,N′-dimethyl-1,2-ethanediamine (60 μl, 49 mg, 0.56 mmol) stirring was continued for another 2 h at 100° C. After cooling down to room temperature, the mixture was poured into saturated aqueous ammonium chloride solution and extracted with dichloromethane. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The crude compound was purified by flash chromatography on silica gel, eluting with ethyl acetate-cyclohexane (1:1 to 1:0) affording the title compound in 64% yield (664 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732600B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3e987077da3849439d683577127ec598
Quellennotizuspto-grants-2010_06