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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332026Generated: October 30, 2026

Hydrochloric Acid → 3-(4-Fluoro-phenyl)-isoxazole-4-carboxylic acid

https://huagongshe.com/reaction/332026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-(4-fluorophenyl)-1,2-oxazole-4-carboxylateHCID 743179—
SolventEthanolHCID 702—
Product3-(4-Fluoro-phenyl)-isoxazole-4-carboxylic acidHCID 2344788594.7%

Reaction Steps

To a solution of 3-(4-fluoro-phenyl)-isoxazole-4-carboxylic acid ethyl ester (849 g, 208 mmol) in ethanol (215 mL) was added aqueous sodium hydroxide (2 N, 161 mL, 323 mmol) and the resulting mixture stirred overnight at room temperature. The mixture was then acidified with HCl solution (4 N, 85 mL) to pH 2-3. The precipitate was then filtered off and dissolved in THF (700 mL) and then washed with saturated sodium chloride solution. The aqueous phase was then extracted with ethyl acetate and THF (1:1, 300 mL) and the combined organic phases dried over sodium sulfate and evaporated to afford the title compound (40.8 g, 94%) which was obtained as an orange solid. MS: m/e=206.1 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877782B2
Source datasetuspto-grants-2014_11
ORD IDord-1a9d42c01289436b819de164bd8a20cb
Source noteuspto-grants-2014_11