Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-tert-Butylstyrene | HCID 15627 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86759274 | HCID 86759274 | — |
Reaction Steps
With the use of 100 g (0.567 mole) of p-tert-butoxystyrene and 5.3 g (0.03 mole) of p-tert-butylstyrene, the same polymerization reaction and after-treatment as described in Production Example 2-(1) were conducted. Then, the resulting viscous resinous material was dissolved in 300 g of acetone and poured into 2000 ml of 50% aqueous methanol solution and precipitated resin was subjected to decantation. This process step was conducted further twice, and the resultant was dried under reduced pressure to give 94.5 g of poly(p-tert-butoxystyrene/p-tert-butylstyrene) as white powders. Then, 70 g of the polymer was subjected to the same reaction and after-treatment as described in Production Example 9-(1) to give 48.5 g of poly(p-hydroxystyrene/p-tert-butylstyrene) as white powders. A ratio of p-hydroxystyrene unit and p-tert-butylstyrene unit was about 94:6 by 1HNMR. Mw: about 16000, Mw/Mn: 1.29 (GPC method: polystyrene as standard).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06656660B1 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-fa3f744e22c74ba58e4a85ae1a5fdd17 |
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| Source note | uspto-grants-2003_12 |
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