Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentadiene | HCID 7612 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Product | HCID 22717329 | HCID 22717329 | 9% |
Reaction Steps
As in Example 1, 1,3-cyclopentadiene (1.00 g, 15.13 mmol), trichlorosilane (8.19 g, 60.47 mmol) and tetrabutylphosphonium chloride (0.44 g, 1.49 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 10 hours. The resulting mixture was distilled to yield 0.45 g (yield: 9%) of 2,4-bis(trichlorosilyl)-1-pentene.
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-7c08567cbd2c4975a816671aff68c604 |
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| Source note | uspto-grants-2004_05 |
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