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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510459Generated: November 3, 2026

Hydroxyamine hydrochloride → Ethyl 5-(4-tert-butylphenyl)-1,2-oxazole-3-carboxylate

https://huagongshe.com/reaction/1510459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantEthyl 4-(4-tert-butylphenyl)-2,4-dioxobutanoateHCID 43186901—
SolventEthanolHCID 702—
ProductEthyl 5-(4-tert-butylphenyl)-1,2-oxazole-3-carboxylateHCID 20534825—

Reaction Steps

Hydroxylamine hydrochloride (6.14 g, 88.0 mmol) was added to a suspension of ethyl 4-(4-tert-butylphenyl)-2,4-dioxobutanoate (20.4 g, 73.7 mmol) in absolute ethanol (300 mL) and the reaction was heated to reflux for 3 hours. After cooling to room temperature, the organics were removed in vacuo and the resulting residue was purified by silica gel chromatography, eluting with heptane to 10% methanol in dichloromethane, to obtain afford the title compound white solid was filtered, washed with water and cold ethanol and dried in vacuo to obtain ethyl 5-(4-tert-butylphenyl)isoxazole-3-carboxylate (15.9 g, 58.0 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211927B2
Source datasetuspto-grants-2012_07
ORD IDord-5f60039cd4224f06ac7d8fa176601e6f
Source noteuspto-grants-2012_07