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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975890Generated: November 3, 2026

Azobisisobutyronitrile → t-Butyl maleimide t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 2-hydroxyethyl 5-norbornene-2-carboxylate

https://huagongshe.com/reaction/1975890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant2-Hydroxyethyl bicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 12033823—
Reactant1H-Pyrrole-2,5-dione, 3-(1,1-dimethylethyl)-HCID 12229417—
Reactantt-Butyl bicyclo[2,2,2]oct-5-ene-2-carboxylateHCID 18413667—
SolventTetrahydrofuranHCID 8028—
Productt-Butyl maleimide t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 2-hydroxyethyl 5-norbornene-2-carboxylateHCID 8675664875%

Reaction Steps

t-butyl maleimide (1 mol.), t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate (0.5 mol.), and 2-hydroxyethyl 5-norbornene-2-carboxylate (0.5 mol.) were dissolved in 50 g to 300 g of tetrahydrofuran (THF), 2 g to 15 g of 2,2′-azobisisobutyronitrile (AIBN) were added thereto, then the resultant solution was reacted at a temperature of 60° C. to 70° C. in a nitrogen atmosphere for 10 hours. After a high molecular weight was achieved by the reaction, the resultant product was precipitated in an ethyl ether or hexane solvent. The gathered precipitate was dried, and the desired poly(t-butyl maleimide/t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate/2-hydroxyethyl 5-norbornene-2-carboxylate) polymer was obtained at a yield of about 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225020B1
Source datasetuspto-grants-2001_05
ORD IDord-72426b4d5d1e41fbb872ff127f53c17f
Source noteuspto-grants-2001_05