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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591138Generated: November 1, 2026

2-hydroxybenzaldehyde O-methyloxime → Methyl 2-(2-methoxyiminomethylphenoxymethyl)phenylglyoxylate O-methyloxime

https://huagongshe.com/reaction/1591138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-hydroxybenzaldehyde O-methyloximeHCID 523240—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 2-[2-(bromomethyl)phenyl]-2-(methoxyimino)acetateHCID 54028047—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(2-methoxyiminomethylphenoxymethyl)phenylglyoxylate O-methyloximeHCID 53961752—

Reaction Conditions

Temperature100 °C

Reaction Steps

3.0 g (20 mmol) of 2-hydroxybenzaldehyde O-methyloxime are dissolved in 20 ml of methanol, and 3.6 g (20 mmol) of sodium methanolate (30% strength in methanol) are added. The mixture is refluxed for four hours and then concentrated. The residue is taken up in 100 ml of dimethylformamide, and 6.5 g (23 mmol) of methyl 2-bromomethylphenylglyoxylate O-methyloxime in 50 ml of dimethylformamide are added. The mixture is stirred at 100° C. for 5 hours, the solvent is stripped off, and the residue is taken up in ethyl acetate. The organic phase is washed with water, dried and concentrated. The residue is triturated with pentane to induce crystallization. 4.8 g (67% of theory) of the title compound are obtained in the form of colorless crystals (melting point 73°-76° C., compound no. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206266
Source datasetuspto-grants-1993_04
ORD IDord-b2d5b3c075ea450e89e5767d59c6b665
Source noteuspto-grants-1993_04