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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227146Generated: October 30, 2026

2-Hydroxy-4-Methoxybenzaldehyde → HCID 178515945, compound

https://huagongshe.com/reaction/2227146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy-4-MethoxybenzaldehydeHCID 69600—
ReactantEthylacetate methanolHCID 21584119—
ReactantHCID 135744196HCID 135744196—
SolventEthanolHCID 702—
ProductHCID 178515945HCID 178515945—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 13.6 g (0.0517 mol) of N-Mono[4-(diethylamino)salicylidene]-2-methylpropane-1,2-diamine from Example 1 in 50 ml of ethanol is heated with stirring at 50° C. until a clear solution is obtained. 7.87 g (0.0517 mol) of 4-methoxysalicylaldehyde (solid) are added and the mixture is heated at reflux for 2 h. After that time the reaction is complete (TLC monitoring, ethyl acetate/methanol 9:1). Thereafter the reaction solution is carefully concentrated and the residue is dried under a high vacuum. The crude product obtained comprises 20 g of a dark red oil, which slowly solidifies. Purification is by column chromatography (eluent mixture: ethyl acetate/methanol 9:1). The asymmetrically substituted salen derivative is isolated as the diastereomer mixture (structures I and II). Yield: 7 g, reddish oil (34%). The product is characterized by 1H and 13C NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413926B2
Source datasetuspto-grants-2002_07
ORD IDord-6407da8ad75e4163a130cb36e8700f78
Source noteuspto-grants-2002_07