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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962924Generated: November 1, 2026

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

https://huagongshe.com/reaction/962924

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 numberUS05760244
Source datasetuspto-grants-1998_06
ORD IDord-350bf05947a1475191c1e6e7416faf16
Source noteuspto-grants-1998_06