Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Ethoxydimethylsilane | HCID 61772 | — |
| Reactant | 1,1-Diethenyl-1,3,3,3-tetramethyldisiloxane | HCID 17760531 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Phenethyldimethylethoxysilane | HCID 54188620 | 74.5% |
Reaction Steps
312 mg Of styrene and 312 mg of dimethylethoxysilane were placed in a glass reaction tube and 0.006 ml of acetic acid was added. Then, 0.001 ml of a toluene solution of a 0-valent platinum complex of divinyltetramethyldisiloxane (platinum content: 0.4 Wt. %) was added to this mixture. The reaction tube was sealed with Teflon tape and heated for 30 minutes in an oil bath at 41° C. When the tube contents were analyzed by GC-MS following cooling, the conversion rate of styrene was 80% and phenethyldimethylethoxysilane was produced at a yield of 74.5%. The yield of (α-methylbenzyl) dimethylethoxysilane was 5.5%
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-6cae0fa4808f4dec9469ef7ebe341a55 |
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| Source note | uspto-grants-2000_04 |
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