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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971831Generated: October 25, 2026

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

https://huagongshe.com/reaction/971831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(dimethylamino)dimethylsilaneHCID 77384—
Reactant2,5-Dimethylhexane 2,5-dihydroperoxideHCID 520470—
SolventDiethyl EtherHCID 3283—
Product3,3,6,6,9,9-Hexamethyl-1,2,4,5-tetraoxa-3-silacyclononaneHCID 2131191997.8%

Reaction Conditions

Temperature16 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04161485
Source datasetuspto-grants-1979_07
ORD IDord-ce90ff2921424486a3dd2f34914212c2
Source noteuspto-grants-1979_07