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HRID 1730640Erstellt: 25. Oktober 2026

Acetic Acid → 3,5-Di-tert.butyl-4-hydroxybenzyl-malonic acid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester

https://huagongshe.com/reaction/1730640

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktLithium amideHCID 24532—
EduktPhenol, 4-[(dimethylamino)methyl]-2,6-bis(1,1-dimethylethyl)-HCID 66609—
EduktBis(2,2,6,6-tetramethylpiperidin-4-yl) propanedioateHCID 1244568—
LösungsmittelTolueneHCID 1140—
Produkt3,5-Di-tert.butyl-4-hydroxybenzyl-malonic acid-bis(2,2,6,6-tetramethyl-4-piperidinyl)esterHCID 14093876—

Reaktionsschritte

26 g (0.068 mole) of bis-(2,2,6,6-tetramethyl-4-piperidinyl) malonate and 17.8 g (0.068 mole) of N-(3,5-di-tert.butyl-4-hydroxybenzyl)dimethylamine are dissolved in 200 ml of toluene. After the addition of 0.5 g of lithium amide, the mixture is refluxed for 3 hours. After cooling, the mixture is neutralised with 1.5 ml of 1% acetic acid, and the organic phase repeatedly washed with water. After drying phase repeatedly washed with water. After drying over Na2SO4, the solution is concentrated in vacuo to obtain, as oily residue, 3,5-di-tert.butyl-4-hydroxybenzyl-malonic acid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03993655
Quelldatensatzuspto-grants-1976_11
ORD IDord-8fc656c33893467281e6e931b34dddb2
Quellennotizuspto-grants-1976_11