Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | Methyltriacetoxysilane | HCID 77929 | — |
| Reactant | 1,1-Diethenyl-1,3,3,3-tetramethyldisiloxane | HCID 17760531 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Phenethyltriethoxysilane | HCID 11097560 | 96% |
Reaction Steps
130 mg Of styrene and 217 mg of triethoxysilane were placed in a glass reaction tube and 0.0032 mg of methyltriacetoxysilane was added. Next, 0.0045 ml of a toluene solution of a 0-valent platinum complex of divinyltetramethyldisiloxane (platinum content: 0.04 Wt. %) was added to this mixture. The reaction tube was sealed with Teflon tape and heated for 30 minutes in an oil bath at 50° C. When the tube contents were analyzed by GC-MS following cooling, the conversion rate of styrene was 98% and phenethyltriethoxysilane was produced at a yield of 96%. The yield of (α-methylbenzyl) triethoxysilane was 0.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06048994 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-5c0db5fc7a6e49d3a1e6b2a29f4f430d |
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| Source note | uspto-grants-2000_04 |
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