Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Trimethoxysilane | HCID 17215 | — |
| Reactant | 1,3-Divinyltetramethyldisiloxane | HCID 75819 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Product | HCID 18468823 | HCID 18468823 | — |
Reaction Steps
A siloxane according to the present invention was prepared by charging a flask with 55.8 g (0.3 mole) of 1,3-divinyl-1,1,3,3-tetramethyldisiloxane under a nitrogen atmosphere. A platinum/vinylsiloxane catalyst, prepared according to the method described by Hitchcock et al.(Angew. Chem. Int. Ed. Engl., 30, 1991) was added at a level of 10−6 equivalent of platinum. Acetic acid (0.06 g; 0.001 mol) was introduced and the reaction mixture heated to 60° C. Trimethoxysilane (12.2 g; 0.1 mol) and 0.24 g (0.004 mol) acetic acid were added to an addition funnel and this mixture was slowly added to the flask while the temperature was maintained below 70° C. Subsequently, the reaction mixture was kept at 70° C. for 1 hr. The product was isolated by fractional distillation at 80° C./8 mm Hg to obtain a mixture (confirmed by NMR) of 7% of an α-adduct (1-vinyl-3-(1-trimethoxysilylethyl)-1,1,3,3-tetramethyldisiloxane) having the structure
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420485B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-876bd57cfbf74b86b827e93893e530fa |
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| Source note | uspto-grants-2002_07 |
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