Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1-Ethenyl-4-methylbenzene | HCID 12161 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Styrene p-methylstyrene | HCID 19702659 | 14% |
Reaction Steps
To a glass bottle capped with a septum and flushed with nitrogen were added: 20 cc of purified toluene, 3.0 cc of purified styrene, 2.0 cc of purified p-methylstyrene, 2.8 mmol of TMA, 0.7 cc (1.412 mmol) of [(n-C4H9)3Sn]2O, and 0.0045 mmol of C5H5TiCl3. The mixture was stirred by a magnet stirrer for 22 h at 25° C. Then the content of the bottle was mixed with excess of isopropanol and 0.66 g of amorphous styrene-p-methylstyrene copolymer (yield ca. 14%) was recovered by filtration. The copolymer had a softening point of 122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05326837 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-2b9e00270ef748aeba17d422b13eacf1 |
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| Source note | uspto-grants-1994_07 |
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