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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 971831생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/971831

반응식

참여 물질

역할이름HCID투입량
반응물Bis(dimethylamino)dimethylsilaneHCID 77384—
반응물2,5-Dimethylhexane 2,5-dihydroperoxideHCID 520470—
용매Diethyl EtherHCID 3283—
생성물3,3,6,6,9,9-Hexamethyl-1,2,4,5-tetraoxa-3-silacyclononaneHCID 2131191997.8%

반응 조건

온도16 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04161485
출처 데이터셋uspto-grants-1979_07
ORD IDord-ce90ff2921424486a3dd2f34914212c2
출처 메모uspto-grants-1979_07