HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757026Generated: October 28, 2026
Hydroquinone → Vinylphenol tert-butyl methacrylate 2-vinylnaphthalene
https://huagongshe.com/reaction/1757026
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | tert-Butyl methacrylate | HCID 11448 | — |
| Reactant | 2-Vinylnaphthalene | HCID 13230 | — |
| Reactant | 1-Vinylnaphthalene | HCID 70004 | — |
| Reactant | 2-Ethenylphenol | HCID 135442 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Vinylphenol tert-butyl methacrylate 2-vinylnaphthalene | HCID 67781865 | — |
Reaction Steps
5.54 g (0.05 mol) of vinylphenol, 5.47 g (0.04 mol) of tert-butyl methacrylate, 2.37g (0.02 mol) of 2-vinylnaphthalene and 0.8205 g (5 mol %) of AIBN were charged into 50g (1.7 M) of toluene. After the mixture was stirred at 80° C. for 11 hours, hydroquinone was added and the polymerization was stopped. Toluene was evaporated by an evaporator to prepare a THF solution, and reprecipitation was repeated using cyclohexane. The polymer thus refined was dried in a vacuum baking oven at 40° C. for 14 hours. There was obtained a polymer having a molecular weight of 12,000, a degree of dispersion of 1.87 and a vinylphenol:tert-BuMA:vinylnaphthalene ratio of 52:43:18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05443690 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-54006827c7ed4a78a00ff36a4c140926 |
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| Source note | uspto-grants-1995_08 |
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