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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432339Generated: October 25, 2026

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

https://huagongshe.com/reaction/432339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactant1-(4-Bromoanilino)-3-phenyl-2-propanolHCID 22347200—
SolventDichloromethaneHCID 6344—
Product5-Benzyl-3-(4-bromophenyl)-1,3-oxazolan-2-oneHCID 22346739121.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-488c61f5f95c4a898b00b7ace6810998
Source noteuspto-grants-2003_12