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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299713Generated: October 25, 2026

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

https://huagongshe.com/reaction/2299713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrileHCID 85308279—
SolventWaterHCID 962—
Productmethyl E-2-hydroxyimino-2-(3-phenoxylphenyl)acetateHCID 8658977133%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495581B1
Source datasetuspto-grants-2002_12
ORD IDord-67c53a2e08644fa7b01b9d74d6be868a
Source noteuspto-grants-2002_12