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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 584385Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/584385

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
PatentnummerUS06924300B2
Quelldatensatzuspto-grants-2005_08
ORD IDord-2b41ece8d71e4fb6b3c7eadcd86174d1
Quellennotizuspto-grants-2005_08