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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926557Generated: October 25, 2026

Azobisisobutyronitrile → Hydroxystyrene

https://huagongshe.com/reaction/1926557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactanttert-Butyl acrylateHCID 15458—
Reactant4-Ethenylphenyl acetateHCID 75821—
Reactant3-Hydroxy-1-methacryloyloxyadamantaneHCID 11856523—
SolventTetrahydrofuranHCID 8028—
ProductHydroxystyreneHCID 138202—

Reaction Steps

To a round bottom flask equipped with condenser, thermometer, an argon (Ar) inlet, and a magnetic stirrer bar, the following were added: 4-acetoxystyrene monomer (2.43 grams (g), 0.015 mole), t-butyl acrylate monomer (1.6 g, 0.0125 mole), 3-hydroxy-1-adamantyl methacrylate monomer (5.319 g, 0.0225 mole), 2,2′-azobis(2-methylpropionitrile) (AIBN)(0.328 g, 4% of total moles of monomers), and approximately 40 g of tetrahydrofuran (THF). The reaction mixture was stirred at room temperature and bubbled with Ar flow for 45 minutes before it was heated. The reaction was carried out overnight at 72° C. under an inert Ar atmosphere. The rest of the synthetic procedures are the same as Example 1, except approximately 5 g of concentrated NH4OH was used in deprotecting the acetoxy groups from acetoxystyrene repeat units to form hydroxyl styrene repeat units of the terpolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08182978B2
Source datasetuspto-grants-2012_05
ORD IDord-5c2b9561a3cc46488d806c83fa21991d
Source noteuspto-grants-2012_05