HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968046Generated: October 27, 2026
Azobisisobutyronitrile → 2-(Toluene-4-sulfonyloxy)ethyl acrylate 2-hydroxyethyl methacrylate
https://huagongshe.com/reaction/968046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | Glycidyl methacrylate | HCID 7837 | — |
| Reactant | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| Reactant | 2-(Toluene-4-sulfonyloxy)ethyl acrylate | HCID 22292251 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Toluene-4-sulfonyloxy)ethyl acrylate 2-hydroxyethyl methacrylate | HCID 86759870 | 65% |
Reaction Steps
In a 500 ml round-bottom flask was placed 0.33 mole of 2-(toluene-4-sulfonyloxy)ethyl acrylate, 0.2 mole of 2-hydroxyethyl methacrylate, 0.15 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 ethylether or n-hexane, filtered and dried to provide poly [2-(toluene-4-sulfonyloxy)ethyl acrylate/2-hydroxyethyl methacrylate/-methyl methacrylate/-glycidyl methacrylate] represented by the following chemical formula 6, 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-aa389fd412014a9fb47ca2e135a317f4 |
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| Source note | uspto-grants-2005_10 |
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