Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | Trimethoxysilane | HCID 17215 | — |
| Reactant | Cyclohexane, 1,2,4-triethenyl- | HCID 96529 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Product | HCID 21439246 | HCID 21439246 | — |
| Product | HCID 66694494 | HCID 66694494 | — |
| Product | HCID 69670692 | HCID 69670692 | — |
Reaction Steps
(2-Triethoxysilylethyl)divinylcyclohexane was prepared from triethoxysilane and 1,2,4-trivinylcyclohexane using the procedure disclosed in Example 1 of U.S. Pat. No. 7,696,269 for trimethoxysilane and 1,2,4-trivinylcyclohexane. A 5 liter, three-neck round bottomed flask fitted with a heating mantle, mechanical stirrer, addition funnel, Friedrich condenser, nitrogen inlet and thermocouple/temperature controller was charged with 1800 g TVCH (11.1 moles) and 3.6 g of a solution (1 wt % Pt) of Karstedt's platinum catalyst in xylene. The contents of the flask were stirred and heated to 90° C. Triethoxysilane (1641 g, 9.99 moles), which had been placed in the addition funnel, was then added slowly over a four hour period to control the exotherm. The temperature remained between 101-109° C. during the addition. The SiH/Vinyl molar ratio in the reaction was 1:3. GC analysis of the crude reaction product gave 21 wt % unreacted TVCH, 48 wt % mono-hydrosilylated product, ((2-Triethoxysilylethyl)divinylcyclohexane), 26.3 wt % bis ((2-Triethoxysilylethyl)vinylcyclohexane and 2.7 wt % tris ((2-Triethoxysilylethyl)cyclohexane. The gravimetric ratio of mono to bis was 1.82.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895770B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-77533884fd6b4a2590e286bc0fe87273 |
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| Source note | uspto-grants-2014_11 |
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