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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968052Generated: October 25, 2026

Azobisisobutyronitrile → 2-(Toluene-4-sulfonyloxy)ethyl methacrylate 3-hydroxypropyl methacrylate

https://huagongshe.com/reaction/968052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMethyl MethacrylateHCID 6658—
ReactantGlycidyl methacrylateHCID 7837—
Reactant3-Hydroxypropyl methacrylateHCID 17694—
Reactant2-(Toluene-4-sulfonyloxy)ethyl methacrylateHCID 14344249—
SolventTetrahydrofuranHCID 8028—
Product2-(Toluene-4-sulfonyloxy)ethyl methacrylate 3-hydroxypropyl methacrylateHCID 8675987665%

Reaction Conditions

Temperature67.5 °C

Reaction Steps

In a 500 ml round-bottom flask was placed 0.3 mole of 2-(toluene-4-sulfonyloxy)ethyl methacrylate, 0.22 mole of 3-hydroxypropyl 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 ethyl ether or n-hexane, filtered and dried to provide poly [2-(toluene-4-sulfonyloxy)ethyl methacrylate/3-hydroxypropyl methacrylate-/methyl methacrylate-/glycidyl methacrylate] represented by the following chemical formula 13, at a yield of 65-70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956091B2
Source datasetuspto-grants-2005_10
ORD IDord-a0c7d765352045bc8b57acd008bb8d34
Source noteuspto-grants-2005_10