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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388146Generated: November 2, 2026

Ethanol → Ethyl 5-methyl-3-phenylisoxazole-4-carboxylate

https://huagongshe.com/reaction/2388146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant5-Methyl-3-phenylisoxazole-4-carboxylic acidHCID 14343—
ReactantThionyl ChlorideHCID 24386—
ProductEthyl 5-methyl-3-phenylisoxazole-4-carboxylateHCID 70838—

Reaction Steps

A mixture of 5-methyl-3-phenyl-isoxazole-4-carboxylic acid (10.0 g, 0.05 mol) and thionyl chloride (18.0 ml, 0.25 mol) in ethanol (100 ml) was refluxed for 5 h before it was cooled to room temperature and concentrated in vacuo. The residue was partitioned between ethyl acetate and water, the organic layer was washed with saturated aqueous sodium bicarbonate solution, and brine, before it was dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound as a yellow solid (10.24 g): 1H NMR (CDCl3, 200 MHz): δ=7.61 (m, 2H), 7.43 (m, 3H), 4.25 (q, J=7.0 Hz, 2H), 2.73 (s, 3H), 1.23 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269008B2
Source datasetuspto-grants-2012_09
ORD IDord-07b71e6733c74e4aa4e89b177b266bf0
Source noteuspto-grants-2012_09