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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374305Generated: October 25, 2026

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

https://huagongshe.com/reaction/374305

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 numberUS05166399
Source datasetuspto-grants-1992_11
ORD IDord-a603bb90994b49609cfa9dee60e5aa27
Source noteuspto-grants-1992_11