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HRID 52755Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/52755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Dimethylamino)BenzaldehydeHCID 7479—
EduktPiperidineHCID 8082—
Edukt2,6-Di-tert-butylphenolHCID 31405—
EduktToluene hexaneHCID 21889329—
LösungsmittelO-XyleneHCID 7237—
Produkt2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenolHCID 4066737—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616774
Quelldatensatzuspto-grants-1997_04
ORD IDord-beb031635aaa49749c8a2909d1afb736
Quellennotizuspto-grants-1997_04