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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMethyl MethacrylateHCID 6658—
ReactantGlycidyl methacrylateHCID 7837—
Reactant2-Hydroxyethyl MethacrylateHCID 13360—
Reactant2-(Toluene-4-sulfonyloxy)ethyl acrylateHCID 22292251—
SolventTetrahydrofuranHCID 8028—
Product2-(Toluene-4-sulfonyloxy)ethyl acrylate 2-hydroxyethyl methacrylateHCID 8675987065%

Reaction Conditions

Temperature67.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956091B2
Source datasetuspto-grants-2005_10
ORD IDord-aa389fd412014a9fb47ca2e135a317f4
Source noteuspto-grants-2005_10