HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099000Generated: November 1, 2026
1-Ethenyl-4-methylbenzene → 1-Methyl-4-[2-(trichlorosilyl)ethyl]benzene
https://huagongshe.com/reaction/1099000
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethenyl-4-methylbenzene | HCID 12161 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Catalyst | Phenothiazine | HCID 7108 | — |
| Product | 1-Methyl-4-[2-(trichlorosilyl)ethyl]benzene | HCID 12159472 | 98% |
Reaction Steps
Into a 3 liter round-bottom flask fitted with a reflux condenser, addition funnel and magnetic stir bar, was charged 4-methylstyrene (904.4 g, 7.65 mols), VCAT (2.25 g, 50 ppm) and phenothiazine (1.94 g, 1000 ppm). The reaction mixture was heated to 70° C. and then trichlorosilane (1036.6 g, 7.65 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, >98% pure (2-p-tolyl-ethyl)trichlorosilane (1565 g, 6.19 mols) was obtained (collected at 75° C./1 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-2ec0be95778d488ea8a957fdc208569d |
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| Source note | uspto-grants-2012_03 |
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