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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52755Generated: October 25, 2026

4-(Dimethylamino)Benzaldehyde → 2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenol

https://huagongshe.com/reaction/52755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Dimethylamino)BenzaldehydeHCID 7479—
ReactantPiperidineHCID 8082—
Reactant2,6-Di-tert-butylphenolHCID 31405—
ReactantToluene hexaneHCID 21889329—
SolventO-XyleneHCID 7237—
Product2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenolHCID 4066737—

Reaction Steps

To 30.4 g (0.2 mol) of 4-dimethylaminobenzaldehyde in 100 ml of xylene, 39.1 g (0.46 mol) of piperidine is added dropwise over a period of six minutes. The mixture is heated at reflux using a Dean-Stark trap until the separation of water is complete. To the cooled reaction mixture 40.3 (0.2 mol) of 2,6-di-tert-butylphenol in 70 ml of xylene is added rapidly. The mixture is then heated at reflux for five hours. The title compound is isolated as an almost white solid by evaporation of the solvent and recrystallization from toluene-hexane. The yield is 66.3 g of the title compound, melting at 184°-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616774
Source datasetuspto-grants-1997_04
ORD IDord-beb031635aaa49749c8a2909d1afb736
Source noteuspto-grants-1997_04