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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584385Generated: October 25, 2026

Hydrochloric Acid → methyl (4E)-4-[(4-hydroxyphenyl)methoxyimino]-4-phenylbutanoate

https://huagongshe.com/reaction/584385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzenebutanoic acid, gamma-oxo-, methyl esterHCID 141190—
ReactantSodium AcetateHCID 517045—
Reactant4-MethoxymethoxybenzyloxyamineHCID 11052292—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventEthyl acetate hexaneHCID 21226206—
Productmethyl (4E)-4-[(4-hydroxyphenyl)methoxyimino]-4-phenylbutanoateHCID 1094692950%

Reaction Steps

A mixture of 4-methoxymethoxybenzyloxyamine (4.99 g), methyl 4-oxo-4-phenylbutyrate (5.71 g), acetic acid (5.10 ml), sodium acetate (4.87 g) and methanol (200 ml) was heated under reflux for 15 hours. The reaction mixture was cooled to room temperature, dilute hydrochloric acid was added to the residue and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was dissolved in tetrahydrofuran (50 ml) and methanol (5 ml). To this solution was added 1N hydrochloric acid (10 ml) and heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, water was added and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain methyl E-4-(4-hydroxybenzyloxyimino)-4-phenylbutyrate (4.24 g, yield 50%) as a colorless oil from an ethyl acetate-hexane (2:5, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924300B2
Source datasetuspto-grants-2005_08
ORD IDord-2b41ece8d71e4fb6b3c7eadcd86174d1
Source noteuspto-grants-2005_08