Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | 1,1-Diethenyl-1,3,3,3-tetramethyldisiloxane | HCID 17760531 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Phenethyltriethoxysilane | HCID 11097560 | 13% |
Reaction Steps
130 mg Of styrene and 217 mg of triethoxysilane were placed in a glass reaction tube and 0.0015 ml of acetic anhydride 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 16% and phenethyltriethoxysilane was produced at a yield of 13%. The yield of (α-methylbenzyl) triethoxysilane was 2%.
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-02bbf50ad32f482b80068c1b51de8090 |
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| Source note | uspto-grants-2000_04 |
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