Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381484Generated: October 26, 2026

4-(Dimethylamino)Benzaldehyde → (4-(4-(4-Dimethylaminobenzyliden-1-yl)-3-methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid

https://huagongshe.com/reaction/1381484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Dimethylamino)BenzaldehydeHCID 7479—
Reactant4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acidHCID 109029—
SolventEthanolHCID 702—
Product(4-(4-(4-Dimethylaminobenzyliden-1-yl)-3-methyl-5-oxo-2-pyrazolin-1-yl)benzoic acidHCID 776848—

Reaction Steps

A slurry composed of 1-(4-carboxyphenyl)-3-methyl-2-pyrazolin-5-one (21.8 gm, 0.10 mol), 4-dimethylaminobenzaldehyde (14.9 gm, 0.10 mol) and EtOH (250 ml) was heated at reflux for two hours. The reaction mixture was cooled to RT resulting in a crude orange product which was isolated by filtration. The product was then washed with ether and dried. The product was purified further by making a slurry of the solid in EtOH (700 ml) at refluxing temperature and filtering the slurry to recover the dye. The treatment was repeated. The mp of the product was above 310° C. The NMR and IR spectra were consistent with the structure assigned. The C,H, and N elemental analyses were in agreement with those calculated for the empirical formula.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803150
Source datasetuspto-grants-1989_02
ORD IDord-d792f146e30a482c89875bf2a224fc57
Source noteuspto-grants-1989_02