HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418124Generated: October 26, 2026
Chlorodimethylsilane → Silane, tetrakis[2-(chlorodimethylsilyl)ethyl]-
https://huagongshe.com/reaction/1418124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodimethylsilane | HCID 66108 | — |
| Reactant | Tetravinylsilane | HCID 66188 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Silane, tetrakis[2-(chlorodimethylsilyl)ethyl]- | HCID 11016725 | — |
Reaction Steps
Under argon, 234.2 g (2.475 mol) chlorodimethyl silane, 500 ml TBME and 1.5 g catalyst 1 were added to 75 g (0.550 mol) tetravinyl silane. The reaction mixture was heated, with vigorous stirring, to 45° C. until an exothermic reaction set in and the temperature rose to 51° C. A mixture comprising 525 g (3.853 mol) tetravinyl silane, 1639.4 g (17.327 mol) chlorodimethyl silane and 940 ml TBME was then added slowly dropwise, wherein care was taken that the reaction temperature did not fall below 50° C. Stirring was then continued for 1.5 hours under reflux, the reaction mixture was cooled to room temperature, the catalyst was filtered off over a frit, and volatile constituents were removed from the colourless solution under vacuum. The product took the form of a white solid. Yield: 2120.8 g (94% of theoretical yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05880305 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-ca94177efee148488a6dd31b7fda853e |
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| Source note | uspto-grants-1999_03 |
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