HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-ethyl-2-adamantyl Methacrylate p-hydroxystyrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | 2-Ethyl-2-methacryloyloxyadamantane | HCID 9813645 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-ethyl-2-adamantyl Methacrylate p-hydroxystyrene | HCID 22508392 | — |
Reaction Steps
Into a flask were charged 250 g of the copolymer of 2-ethyl-2-adamantyl methacrylate and p-acetoxystyrene (20:80) obtained in Synthesis Example 3, 10.3 g (0.084 mol) of 4-dimethylaminopyridine and 202 g of methanol, and aged for 20 hours under reflux. After cooling, the reaction liquid was neutralized with 7.6 g (0.126 mol) of glacial acetic acid and poured into a large amount of water to precipitate a polymer. The deposited polymer was filtrated, dissolved in acetone, then, poured into a large amount of water to cause precipitation, and this operation was repeated three times in total for purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202010B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-b4bc4c4c1f984d2b85579eace7e62e4e |
| Source note | uspto-grants-2007_04 |