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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860695Generated: November 1, 2026

Hydrochloric Acid → HCID 58765719, compound

https://huagongshe.com/reaction/860695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58765662HCID 58765662—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58765719HCID 58765719—

Reaction Steps

3-(2-Methyl-4-{2-[5-methyl-2-(4-pyridin-2-yl-phenyl)-oxazol-4-yl]-propoxy}-phenyl)-propionic acid methyl ester from step A is dissolved in tetrahydrofuran (1 mL) and 5N sodium hydroxide (1 mL) solution is added with stirring at room temperature. The reaction is heated to reflux and monitored by HPLC. Upon complete conversion, the reaction is allowed to cool to room temperature and neutralized with 5N hydrochloric acid (1 mL), diluted with ethyl acetate, and extracted. The organic layer is washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The pure 3-(2-Methyl-4-{2-[5-methyl-2-(4-pyridin-2-ylphenyl)oxazol-4yl]propoxy}phenyl)propionic acid (400 mg, 0.875 mmol) may also be obtained by recrystalization from ethyl acetate. 70% yield 2 steps, MS (ES): 457.2 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153878B2
Source datasetuspto-grants-2006_12
ORD IDord-cb3b42829c51430ba7d1daceadd2d9b8
Source noteuspto-grants-2006_12