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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2299713Erstellt: 25. Oktober 2026

Hydrochloric Acid → methyl E-2-hydroxyimino-2-(3-phenoxylphenyl)acetate

https://huagongshe.com/reaction/2299713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
EduktPotassium HydroxideHCID 14797—
Edukt2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrileHCID 85308279—
LösungsmittelWaterHCID 962—
Produktmethyl E-2-hydroxyimino-2-(3-phenoxylphenyl)acetateHCID 8658977133%

Reaktionsschritte

A mixture of 2-hydroxyimino-2-(3-phenoxyphenyl)acetonitrile (3.00 g), potassium hydroxide (3.40 g), ethanol (15 ml) and water (15 ml) was heated under reflux for 24 hours. The reaction mixture was acidified with 1 N HCl, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried (MgSO4) and then concentrated. The reaction mixture was dissolved in methanol (30 ml), admixed with concentrated sulfuric acid (a catalytic amount), and then heated under reflux for 24 hours. The reaction mixture was combined with aqueous sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried (MgSO4) and then concentrated. The residue was subjected to column chromatography on silica gel to obtain methyl Z-2-hydroxyimino-2-(3-phenoxyphenyl)acetate (1.14 g, yield 33%) as an oil from a fraction eluted with ethyl acetate-hexane (1:2, v/v).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06495581B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-67c53a2e08644fa7b01b9d74d6be868a
Quellennotizuspto-grants-2002_12