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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2299743Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2299743

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBenzenebutanoic acid, gamma-oxo-, methyl esterHCID 141190—
EduktSodium AcetateHCID 517045—
Edukt4-MethoxymethoxybenzyloxyamineHCID 11052292—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produktmethyl (4E)-4-[(4-hydroxyphenyl)methoxyimino]-4-phenylbutanoateHCID 1094692950%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06495581B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-bb5ca6f3f4ef4c96ab6478433d29b685
Quellennotizuspto-grants-2002_12