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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432339Erstellt: 24. Oktober 2026

Diisopropylethylamine → 5-Benzyl-3-(4-bromophenyl)-1,3-oxazolan-2-one

https://huagongshe.com/de/reaction/432339

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktTriphosgeneHCID 94429—
Edukt1-(4-Bromoanilino)-3-phenyl-2-propanolHCID 22347200—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Benzyl-3-(4-bromophenyl)-1,3-oxazolan-2-oneHCID 22346739121,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution containing 1-(4-bromoanilino)-3-phenyl-2-propanol (1.90 g, 0.00621 mol), N,N-diisopropylethylamine (2.48 g, 0.0193 mol) and N,N-dimethylaminopyridine (0.152 g, 0.00124 mol) in anhydrous dichloromethane (64 mL) was cooled to 0° C. and the solution of triphosgene (0.92 g, 0.0031 mol) in anhydrous dichloromethane (16 mL) was added dropwise. The reaction mixture was slowly warmed up to ambient temperature while stirring under an atmosphere of nitrogen for 18 hours. The organic phase was washed with saturated solution of sodium bicarbonate in water (70 mL), brine (60 mL) and dried with magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by flash chromatography on silica using ethyl acetate/n-heptane (1:5) as mobile phase to yield 5-benzyl-3-(4-bromophenyl)-1,3-oxazolan-2-one (1.25 g, 0.00377 mol) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660744B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-488c61f5f95c4a898b00b7ace6810998
Quellennotizuspto-grants-2003_12