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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054134Generated: November 2, 2026

Diethyl (ethoxymethylene)malonate → Ethyl 5-oxo-2-phenyl-2,5-dihydroisoxazole-4-carboxylate

https://huagongshe.com/reaction/2054134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantNitrobenzeneHCID 7416—
ReactantN-PhenylhydroxylamineHCID 7518—
ReactantHydrazine hydrate (1:1)HCID 24654—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-oxo-2-phenyl-2,5-dihydroisoxazole-4-carboxylateHCID 11746543—

Reaction Conditions

Temperature27.5 °C

Reaction Steps

Hydrazine hydrate (1.7 g) was added dropwise over 30 min to a stirred suspension of 5% Rh—C (wet, 110 mg) and nitrobenzene (4.1 g) in THF (20 mL) at 15° C. controlled by ice-bath. The reaction mixture was warmed to 25-30° C. for 2 h, followed by filtration. The filtrate was diluted with an equal volume of dichloromethane, dried over sodium sulfate, then condensed to a small volume. Addition of petroleum ether to this solution led to the formation of a needle-like white solid as the fairly pure product of phenyl hydroxyamine (3.2 g, 86%). The reaction mixture of phenyl hydroxyamine (2.675 g, 25 mmol), diethyl ethoxymethylene malonate (4.324 g, 20 mmol) and ethanol (20 mL) was stirred at RT for 12 h to form a large amount of solid, which after warming on a water-bath for 3 h disappeared and reappeared when the reaction mixture was cooled down to RT. Filtration and washing with ethanol provided the title compound as white crystal like solid (4.25 g, 91%). 1H NMR (200 MHz, CDCl3) δ (ppm): 8.40 (s, 1H), 7.46-7.28 (m, 5H), 4.23(q, J=7.1 Hz, 2H). 1.31 (t, J.=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329651B2
Source datasetuspto-grants-2008_02
ORD IDord-ce9eb310c265460b9f5b62d38d193b42
Source noteuspto-grants-2008_02