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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584361Generated: November 4, 2026

Hydrochloric Acid → Ethyl 2-hydroxy-4-(4-hydroxy-3-methoxyphenyl)butanoate

https://huagongshe.com/reaction/1584361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant1,4-DioxaneHCID 31275—
Reactant2-Acetoxy-4-[3-methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]butyronitrileHCID 21224424—
ProductEthyl 2-hydroxy-4-(4-hydroxy-3-methoxyphenyl)butanoateHCID 2122442160%

Reaction Steps

A mixture of 2-acetoxy-4-[3-methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]butyronitrile (2.0 g), 6 N HCl (24 ml) and dioxane (12 ml) was stirred for 4 hours under reflux. The reaction mixture was poured into water, which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), followed by distilling off the solvent. To the resulting oily product was added ethanolic hydrochloric acid (10%, 24 ml), followed by stirring for 1.5 hours under reflux. The reaction mixture was poured into water, which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4), followed by distilling off the solvent. The resulting oily product was subjected to column chromatography on silica gel. From the fraction eluted with ethyl acetate-hexane (1:2, v/v), was obtained ethyl 2-hydroxy-4-(4-hydroxy-3-methoxyphenyl)butanoate (0.73 g, 60%),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932601
Source datasetuspto-grants-1999_08
ORD IDord-98a2914ddded40668da0be361a3fe5cc
Source noteuspto-grants-1999_08