HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098999Generated: November 5, 2026
1-Ethenyl-4-methylbenzene → HCID 22373345, compound
https://huagongshe.com/reaction/1098999
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Ethenyl-4-methylbenzene | HCID 12161 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Product | HCID 22373345 | HCID 22373345 | 72.8% |
Reaction Steps
Into a 3 liter round-bottom flask fitted with a reflux condenser, addition funnel and magnetic stir bar, was charged 4-methylstyrene (900 g, 7.6 mols) and Bis(triphenylphosphine)palladium (II) dichloride (1.8 g, 0.2% wt). The reaction mixture was heated to 70° C. and then trichlorosilane (1031 g, 7.6 mols) was added dropwise to the reaction mixture. During the addition, the reaction mixture was maintained between 80 to 100° C. After the addition was finished, the reaction mixture was kept at 70° C. for additional two hours. After distillation, pure (1-p-tolyl-ethyl)trichlorosilane (1400 g, 5.53 mols) was obtained (collected at 75° C./1 mmHg). The product structure was characterized by GC-MS and 13C NMR (δ˜14 ppm, CDCl3, Cl3Si—CH (CH3)-Ph; δ˜35 ppm, CDCl3, Cl3Si—CH(CH3)-Ph).
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-8f4c7fd74c3c40e295f9dbe389c9c33a |
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| Source note | uspto-grants-2012_03 |
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