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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy-4-MethoxybenzaldehydeHCID 69600—
ReactantHCID 135581365HCID 135581365—
SolventEthanolHCID 702—
ProductHCID 136388372HCID 136388372—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413926B2
Source datasetuspto-grants-2002_07
ORD IDord-a498fe644d474c9abc28dfb03760d9c4
Source noteuspto-grants-2002_07