HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → p-Tert-butoxystyrene p-methylstyrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Ethenyl-4-methylbenzene | HCID 12161 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Reactant | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | p-Tert-butoxystyrene p-methylstyrene | HCID 67612459 | — |
Reaction Steps
2,2′-Azobis(methyl 2-methylpropionate) was added to a mixture of 100 g (0.567 mole) of p-tert-butoxystyrene and 3.54 g (0.03 mole) of p-methylstyrene in 1,4-dioxane, followed by conducting a polymerization reaction at 80° C. for 6 hours under nitrogen gas streams. After cooling, the reaction solution was poured into 5000 ml of aqueous methanol solution to precipitate out. The precipitated polymer was filtered, washed with methanol and dried under reduced pressure to give 92.3 g of poly(p-tert-butoxystyrene/p-methylstyrene) as white powders. A ratio of p-tert-butoxystyrene unit and p-methylstyrene unit was about 95:5 by 1HNMR. Mw was about 20000 and Mw/Mn was 1.90 by GPC measurement using polystyrene as standard.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06656660B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-ecdc3ce1f081466aaa85836965880355 |
| Source note | uspto-grants-2003_12 |