Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Product | 1-Trichlorosilylethylbenzene | HCID 11791289 | 89% |
Reaction Steps
Into a 2-liter round-bottom flask fitted with a reflux condenser, addition funnel and magnetic stir bar, was charged styrene (410 g, 3.94 mols) and Bis(triphenylphosphine)palladium (II) dichloride (1.2 g, 0.3% wt). The reaction mixture was heated to 70° C. and then trichlorosilane (532.8 g, 3.94 mols) was added dropwise to the reaction mixture. During the addition, the reaction mixture was maintained between 80 to 110° C. After the addition was finished, the reaction mixture was kept at 70° C. for additional two hours. After distillation, >98% pure (1-phenylethyl)trichlorosilane (840 g, 99% purity) was obtained (collected at 78° C./3 mmHg). The product structure was characterized by GC-MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143336B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-10790d81dfd54ff3b4966c39405faa84 |
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| Source note | uspto-grants-2012_03 |
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