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HRID 971831Erstellt: 25. Oktober 2026

Bis(dimethylamino)dimethylsilane → 3,3,6,6,9,9-Hexamethyl-1,2,4,5-tetraoxa-3-silacyclononane

https://huagongshe.com/reaction/971831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(dimethylamino)dimethylsilaneHCID 77384—
Edukt2,5-Dimethylhexane 2,5-dihydroperoxideHCID 520470—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3,3,6,6,9,9-Hexamethyl-1,2,4,5-tetraoxa-3-silacyclononaneHCID 2131191997,8%

Reaktionsbedingungen

Temperatur16 °C

Reaktionsschritte

Into a 250 ml flask equipped with a magnetic stirring bar, addition funnel and calcium sulfate drying tube is placed a solution of 10.84g (0.06 mole, 98.66% pure) of 2,5-dimethyl-2,5-dihydroperoxyhexane in 120 ml of anhydrous ether. The solution is cooled to 16° C. and a solution of 8.77g (0.06 mole) of bis(dimethylamino) dimethylsilane in 30 ml of anhydrous ether is added slowly dropwise. The reaction temperature is maintained between 15° and 20° by use of an ice bath and by adjusting the rate of addition. After the addition is complete, the solution is stirred at room temperature for one hour. The solution is filtered to remove a small amount of suspended solid. The solvent is removed by distillation yielding 13.75g of 3,3,6,6,9,9-hexamethyl-1,2,4,5-tetraoxa-3-silacyclononane (theoretical yield 14.05g, 97.9%; A.O. analysis 13.32%, theoretical 13.67%, 97.4% pure). The infrared spectrum of the reaction product of this example is identical to the spectrum of material produced in Example 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04161485
Quelldatensatzuspto-grants-1979_07
ORD IDord-ce90ff2921424486a3dd2f34914212c2
Quellennotizuspto-grants-1979_07