HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848945Generated: October 30, 2026
tert-Butyl methacrylate → HCID 22239517, compound
https://huagongshe.com/reaction/848945
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl methacrylate | HCID 11448 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-Vinylphenol | HCID 62453 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 22239517 | HCID 22239517 | 83.5% |
Reaction Steps
A 500-ml flask was charged with 72.1 g (0.60 mol) of 4-hydroxystyrene, 17.1 g (0.12 mol) of t-butyl methacrylate, 1.5 g (0.009 mol) of azobisisobutyronitrile and 150 ml of dioxane, and the mixture was stirred for 100 hours at 80t in a nitrogen gas stream. The resultant reaction mixture was poured into 5 liters of xylene, and precipitate formed was collected by filtration. The resultant precipitate was dissolved in 200 ml of diethyl ether, and the solution was poured into 3 liters of n-hexane to collect precipitate formed by filtration (reprecipitation process). This reprecipitation process was repeated 3 times, and the resultant precipitate was dried to obtain 26.3 g of a 4-hydroxystyrene/t-butyl methacrylate copolymer. The GPC analysis of the polymer thus obtained revealed that its Mw was 6,410. Besides, the 1H-NMR spectrum analysis of the polymer revealed that the copolymerization ratio of 4-hydroxystyrene to t-butyl methacrylate was 71/29.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06010826 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-edb8644b76ca44e99ed717121447c3e4 |
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| Source note | uspto-grants-2000_01 |
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