HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379283Generated: October 30, 2026
Styrene → 1,1,3,3-TETRAMETHYL-1,3-DI(2-PHENYLETHYL) DISILOXANE
https://huagongshe.com/reaction/379283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Styrene | HCID 7501 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,1,3,3-Tetramethyl-disiloxane | HCID 18659 | — |
| Reactant | Triisopropylsilyl trifluoromethanesulfonate | HCID 2724529 | — |
| Reactant | HCID 125730908 | HCID 125730908 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,1,3,3-TETRAMETHYL-1,3-DI(2-PHENYLETHYL) DISILOXANE | HCID 11427856 | 58% |
Reaction Steps
380 mg Of styrene and 240 mg of 1,1,3,3-tetramethyldisiloxane were placed in a glass tube to which 20 μL (21.6 mg) of acetic anhydride and 2 μL (2.3 mg) of triisopropylsilyl trifluoromethanesulfonate (i-Pr3SiOSO2CF3) were added by microsyringe. 5 μL (platinum weight: 0.0017 mg) Of a toluene solution (platinum content: 0.04 wt %) of zero-valent platinum complexed with divinylsiloxane were added to this. The tube was put in a 60° C. oil bath and heated for 8 hours. After cooling, the tube contents were analyzed by gas chromatography, which revealed that the styrene conversion rate was 55%, 1-phenethyl-1,1,3,3-tetramethyldisiloxane had been produced at a yield of 58% (based on 1,1,3,3-tetramethyldisiloxane) and 1,3-bis(phenethyl)-1,1,3,3-tetramethyldisiloxane at a yield of 21%, and the ratio of alpha addition to beta addition of phenethyl groups was 1:49.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06297340B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-f6c28f084f244659b617837f722b3dab |
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| Source note | uspto-grants-2001_10 |
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