HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848947Generated: October 30, 2026
Azobisisobutyronitrile → HCID 86755013, compound
https://huagongshe.com/reaction/848947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Butyl Methacrylate | HCID 7354 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-Vinylphenol | HCID 62453 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 86755013 | HCID 86755013 | 75% |
Reaction Steps
A 500-ml flask was charged with 72.1 g (0.60 mol) of 4-hydroxystyrene, 17.0 g (0.12 mol) of n-butyl methacrylate, 1.5 g (0.009 mol) of azobisisobutyronitrile and 150 ml of dioxane, and the mixture was stirred for 20 hours at 80° C. 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 solids were 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 then dried to obtain 23.6 g of a 4-hydroxystyrene/n-butyl methacrylate copolymer. The GPC analysis of the polymer thus obtained revealed that its Mw was 5,600. Besides, the 1H-NMR spectrum analysis of the polymer revealed that the copolymerization ratio of 4-hydroxystyrene to n-butyl methacrylate was 68/32.
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-57d36bb1310d4243a7e98e4b93e95fa7 |
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| Source note | uspto-grants-2000_01 |
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