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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968049Generated: October 27, 2026

Azobisisobutyronitrile → 2-(Toluene-4-sulfonyloxy)ethyl acrylate 4-hydroxybutyl acrylate

https://huagongshe.com/reaction/968049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMethyl MethacrylateHCID 6658—
ReactantGlycidyl methacrylateHCID 7837—
Reactant4-Hydroxybutyl acrylateHCID 75588—
Reactant2-(Toluene-4-sulfonyloxy)ethyl acrylateHCID 22292251—
SolventTetrahydrofuranHCID 8028—
Product2-(Toluene-4-sulfonyloxy)ethyl acrylate 4-hydroxybutyl acrylateHCID 8675987365%

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 acrylate, 0.2 mole of 4-hydroxybutyl acrylate, 0.1 mole of methyl methacrylate, 0.3 mole of glycidyl methacrylate, and 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 acrylate/4-hydroxybutyl acrylate/-methyl methacrylate/-glycidyl methacrylate] represented by the following chemical formula 9, at a yield of 65-70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956091B2
Source datasetuspto-grants-2005_10
ORD IDord-d05c1f8488424fec9452cf5bd98f35be
Source noteuspto-grants-2005_10