HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968053Generated: October 25, 2026
Azobisisobutyronitrile → 2-(Toluene-4-sulfonyloxy)ethyl methacrylate 4-hydroxybutyl acrylate
https://huagongshe.com/reaction/968053
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | Glycidyl methacrylate | HCID 7837 | — |
| Reactant | 4-Hydroxybutyl acrylate | HCID 75588 | — |
| Reactant | 2-(Toluene-4-sulfonyloxy)ethyl methacrylate | HCID 14344249 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Toluene-4-sulfonyloxy)ethyl methacrylate 4-hydroxybutyl acrylate | HCID 86759877 | 65% |
Reaction Steps
In a 500 ml round-bottom flask was placed 0.3 mole of 2-(toluene-4-sulfonyloxy)ethyl methacrylate, 0.2 mole of 4-hydroxybutyl acrylate, 0.1 mole of methyl methacrylate, 0.3 mole of glycidyl methacrylate, 300 g of tetrahydrofuran (THF), and 0.1 g-3 g of AIBN. The reaction mixture was heated at 60-75° C. for 5-20 hours. The product was precipitated in ethyl ether or n-hexane, filtered and dried to provide poly [2-(toluene-4-sulfonyloxy)ethyl methacrylate/4-hydroxybutyl acrylate-/methyl methacrylate-/glycidyl methacrylate] represented by the following chemical formula 14, at a yield of 65-70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06956091B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-aa10fa8eeee4476c8a357675d97125bb |
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| Source note | uspto-grants-2005_10 |
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