Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tridecylsilane; | HCID 4168115 | — |
| Reactant | HCID 131722834 | HCID 131722834 | — |
| Product | HCID 4559047 | HCID 4559047 | 94% |
Reaction Steps
The reaction was carried out in a similar manner as described in Example I. A mixture of (n-C10H21)3SiH (25.0 g, 55.3 mmole), (n-C10H21)3SiCH═CH2 (26.4 g, 55.3 mmole) and Pt(acetylacetonate)2 (22 mg, 5.53×10−2 mmole) was placed in the flask. The reaction mixture was stirred at room temperature for two days and then at ˜40° C. for another two days. The product was purified by column chromatography as described in Example I. After removal of the solvent, a crude product was obtained. The crude product was distilled to remove the low boiling components at <230° C./5×10−5 mmHg and yielded the desired product (n-C10H21)3SiCH2CH2Si(n-C10H21)3 (48.4 g, colorless liquid, 94 percent yield). The infrared spectrum and mass spectra data were consistent with the expected structure. In the analysis for C62H130Si2, the amount calculated was: C, 79.91; H, 14.06; Si, 6.03 percent, while the amount found was: C, 80.12; H, 14.15; Si, 5.92 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06278011B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-b217a4c8fbe043a5b7055245ba9e588e |
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| Source note | uspto-grants-2001_08 |
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