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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939642Generated: November 2, 2026

Ethanol → Ethyl 5-ethoxy-4,5-dihydro-1,2-oxazole-3-carboxylate

https://huagongshe.com/reaction/1939642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 54377377HCID 54377377—
ProductEthyl 5-ethoxy-4,5-dihydro-1,2-oxazole-3-carboxylateHCID 1481146276%

Reaction Steps

17.22 g of 4-ethoxy-2-oxo-3-butenoic acid prepared according to the method of L. Tietze et al. (Lutz-F. Tietze, Heinrich Meier and Edgar Voss, Synthesis 1988, 274) are dissolved in 50 ml of anhydrous ethanol, and 7.34 g of hydroxylamine hydrochloride is added thereto, and the mixture is stirred at room temperature for 4 hours. The reaction mixture is added with water and extracted with methylene chloride. The organic layer is washed with water, dried, and evaporated. The resulting residue is distilled under reduced pressure to yield 14.3 g of ethyl 5-ethoxyisoxazoline-3carboxylate. (yield 76%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696271
Source datasetuspto-grants-1997_12
ORD IDord-f84e38c3b16b4d3cb563f12e8fb3a9b9
Source noteuspto-grants-1997_12