Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexadiene | HCID 11602 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Product | HCID 22717334 | HCID 22717334 | 74% |
| Product | HCID 73993291 | HCID 73993291 | 10% |
Reaction Steps
As in Example 1, 1,3-hexadiene (1.00 g, 12.17 mmol), trichlorosilane (6.59 g, 48.65 mmol) and tetrabutylphosphonium chloride (0.36 g, 1.22 mmol) were added in a 25 mL stainless steel tube under nitrogen atmosphere. After sealing the cylinder with a cap, the reactor was maintained at 180° C. for 8 hours. The resulting mixture was distilled to yield 1.64 g (yield: 74%) of 1,1-dichloro-2,5-dimethylsilacyclo-3-pentene and 0.43 g (yield: 10%) of 2,5-bis(trichlorosilyl)-3-hexene main products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740766B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-2d35793a6a124ce39e9777bf5c570979 |
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| Source note | uspto-grants-2004_05 |
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