HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227148Generated: October 30, 2026
2-Hydroxy-4-Methoxybenzaldehyde → HCID 136388372, compound
https://huagongshe.com/reaction/2227148
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Hydroxy-4-Methoxybenzaldehyde | HCID 69600 | — |
| Reactant | HCID 135581365 | HCID 135581365 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136388372 | HCID 136388372 | — |
Reaction Steps
To a suspension of 2.5 g (8.64 mmol) of (R,R)-N-mono[4-(diethylamino)salicylidene]-1,2-cyclohexanediamine in 200 ml of ethanol is added dropwise over the course of 45 minutes at room temperature a solution of 1.3 g (8.64 mmol) of 4-methoxysalicylaldehyde in 200 ml of ethanol. The reaction solution is heated at 60° C. for 4 h. After the reaction solution has been cooled to room temperature it is concentrated to dryness. The crude product obtained is purified by column chromatography (ethyl acetate/methanol 9:1). Yield: 500 mg (14%), reddish orange oil, which slowly crystallizes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413926B2 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-a498fe644d474c9abc28dfb03760d9c4 |
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| Source note | uspto-grants-2002_07 |
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