HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582546Generated: November 1, 2026
2-Hydroxy-4-Methoxybenzaldehyde → HCID 178515945, compound
https://huagongshe.com/reaction/1582546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Hydroxy-4-Methoxybenzaldehyde | HCID 69600 | — |
| Reactant | Ethylacetate methanol | HCID 21584119 | — |
| Reactant | HCID 135744196 | HCID 135744196 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178515945 | HCID 178515945 | — |
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 500° 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06737391B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-13cea135a6884c29ac2070f73db19e59 |
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| Source note | uspto-grants-2004_05 |
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