HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120031Generated: October 25, 2026
Methanol → 2-ethyl-2-adamantyl Methacrylate p-acetoxystyrene
https://huagongshe.com/reaction/2120031
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,1'-Dimethyl 2,2'-(1,2-diazenediyl)bis(2-methylpropanoate) | HCID 75763 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | 2-Ethyl-2-methacryloyloxyadamantane | HCID 9813645 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-ethyl-2-adamantyl Methacrylate p-acetoxystyrene | HCID 86587147 | — |
Reaction Steps
Into a flask were charged 39.7 g (0.16 mol) of 2-ethyl-2-adamantyl methacrylate, 103.8 g (0.64 mol) of p-acetoxystyrene and 265 g of isopropanol, and the mixture was heated up to 75° C. under a nitrogen atmosphere. Into this solution was dropped a solution prepared by dissolving 11.05 g (0.048 mol) of dimethyl 2,2′-azobis(2-methylpropionate) in 22.11 g of isopropanol. The mixture was aged for about 0.3 hours at 75° C., and for about 12 hours under reflux, then, diluted with acetone. The reaction solution was poured into a large amount of methanol to precipitate a polymer which was filtrated. The amount of the resulted copolymer of 2-ethyl-2-admantyl methacrylate and p-acetoxystyrene was 250 g (weight of wet cake containing methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689531B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-b566d380804248c1b39787bf7b7a0245 |
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| Source note | uspto-grants-2004_02 |
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