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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070045Generated: October 31, 2026

Hydrochloric Acid → ethyl (2Z)-2-(3-benzoylphenyl)-2-hydroxyiminoacetate

https://huagongshe.com/reaction/1070045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(3-Benzoylphenyl)-2-(hydroxyimino)acetonitrileHCID 73884348—
SolventEthyl acetate hexaneHCID 21226206—
Productethyl (2Z)-2-(3-benzoylphenyl)-2-hydroxyiminoacetateHCID 8795055414%

Reaction Steps

A mixture of 2-(3-benzoylphenyl)-2-(hydroxyimino)acetonitrile (14.5 g), 4N aqueous solution of potassium hydroxide (80 ml) and ethanol (80 ml) was heated under reflux for 20 hours. The reaction mixture was cooled to room temperature, 1N hydrochloric acid was added to make the solution acidic 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 ethanol (150 ml) and concentrated sulfuric acid (catalytic amount) was added. The reaction mixture was heated under reflux for 15 hours, cooled to room temperature, poured into an aqueous saturated solution of sodium bicarbonate 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 ethyl Z-2-(3-benzoylphenyl)-2-(hydroxyimino)acetate (2.48 g, yield 14%) as a pale-brown oil from an ethyl acetate-hexane (1:2, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-3ad3e1598cf34eaab6c69fa726db1334
Source noteuspto-grants-2001_06