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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1650041Erstellt: 26. Oktober 2026

Sodium Chloride → Di-(1-nonyloxy-2,2,6,6-tetramethylpiperidin-4-yl) Sebacate

https://huagongshe.com/reaction/1650041

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
Edukttert-Butyl hydroperoxideHCID 6410—
EduktTinuvin 770HCID 164282—
KatalysatorVanadium(III) acetylacetonateHCID 5377225—
LösungsmittelNonaneHCID 8141—
ProduktDi-(1-nonyloxy-2,2,6,6-tetramethylpiperidin-4-yl) SebacateHCID 538868027,9%

Reaktionsbedingungen

Temperatur151 °C

Reaktionsschritte

A 2-phase mixture of 85.7 g (0.666 mol) of 70% aqueous tert-butyl hydroperoxide, 200 ml of n-nonane and 10 g of sodium chloride is agitated in a separatory funnel. The organic layer is dried over anhydrous magnesium sulfate. A mixture of 40.0 g (0.0832 mol) of bis-(2,2,6,6-tetramethylpiperidin-4-yl) sebacate and the tert-butyl hydroperoxide solution in n-nonane is heated to reflux (151° C.) under a nitrogen atmosphere. Vanadium (III) acetylacetonate (2.0 g) is added over a 15-minute interval. The reaction mixture is diluted with 50 ml of nonane. The reaction mixture is heated at reflux for 22 hours. Water is collected in a Dean-Stark trap. The mixture turns red and then darkens in color. The solvent is then removed under reduced pressure. The residue is dissolved in 150 ml of heptane and then passed through a short column of silica gel with additional heptane. The crude product is purified by chromatography (Waters Prep 500A HPLC; 29:1 heptane:ethyl acetate) to afford 2.5 g (4% yield) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04921962
Quelldatensatzuspto-grants-1990_05
ORD IDord-7c8d617315e045e49a0e55938b6e814d
Quellennotizuspto-grants-1990_05