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HRID 1590934Erstellt: 24. Oktober 2026

Sodium Chloride → Bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) succinate

https://huagongshe.com/de/reaction/1590934

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
Edukttert-Butyl hydroperoxideHCID 6410—
EduktBis(2,2,6,6-tetramethyl-4-piperidyl) succinateHCID 93340—
KatalysatorMolybdenum oxideHCID 139765—
LösungsmittelCyclohexaneHCID 8078—
ProduktBis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) succinateHCID 21026400137,6%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A two-phase mixture of 70% aqueous t-butyl hydroperoxide (103.9 g, 807 mmol), cyclohexane (200 ml) and sodium chloride (15 g) is shaken in a separatory funnel. The organic phase is dried over magnesium sulfate, filtered, and added to 40.0 g (101 mmol) of di-(2,2,6,6-tetramethylpiperidin-4-yl) succinate. Molybdenum oxide (2.0 g) is added, and the mixture is refluxed for one hour. Water is collected in a Dean-Stark trap. The entire reaction mixture is then transferred to a Fischer-Porter bottle and heated at 140° C. for 6 hours. Additional t-butyl hydroperoxide (90%, 10.1 g, 101 mmol) is added and heating is resumed for another 4 hours. The colorless reaction mixture is filtered, concentrated, and dissolved in heptane (20 0 ml). The heptane solution is passed through a short column of silica gel with heptane. Subsequent evaporation affords an oil which is crystallized from ethanol to yield 41.2 g (69%) of a white powder, m.p. 122°-6° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05204473
Quelldatensatzuspto-grants-1993_04
ORD IDord-a1480b7fb3654dbca29483403b9b58c6
Quellennotizuspto-grants-1993_04