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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38306Generated: October 27, 2026

Ethyl Acetate → 3-(2-Oxo-1,3-oxazolidin-3-yl)benzaldehyde

https://huagongshe.com/reaction/38306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-BromoethanolHCID 10898—
ReactantSodium hydrideHCID 24758—
Reactant3-(BOC-Amino)benzaldehydeHCID 16740736—
SolventDimethylformamideHCID 6228—
Product3-(2-Oxo-1,3-oxazolidin-3-yl)benzaldehydeHCID 2313182429.6%

Reaction Steps

To a solution of 2.93 g of 3-[N-(t-butoxycarbonyl)amino]benzaldehyde in 20 ml of dimethylformamide was added 0.58 g of sodium hydride (60% oily) under ice-cooling. After stirring at room temperature for 1 hour, a solution of 0.93 ml of 2-bromoethanol in 5 ml of dimethylformamide was added dropwise under ice-cooling. After stirring at room temperature for 14 hours, the mixture was heated to stir at 115° C. for 6 hours. Ethyl acetate was added, and this was washed successively with water and an aqueous saturated sedum chloride solution, dried with anhydrous sodium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.75 g of oily 3-(2-oxo-oxazolidin-3-yl)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524729B2
Source datasetuspto-grants-2013_09
ORD IDord-66c3dc5457934a1f8fca48a64bde6623
Source noteuspto-grants-2013_09