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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393499Generated: October 26, 2026

Azobisisobutyronitrile → 2-Hydroxyethyl 5-norbornene-2-carboxylate t-butyl 5-norbornene-2-carboxylate 5-norbornene 2-carboxylic acid maleic anhydride

https://huagongshe.com/reaction/393499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
Reactant5-Norbornene-2-carboxylic acidHCID 78949—
Reactant2-Hydroxyethyl bicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 12033823—
ReactantBicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 1,1-dimethylethyl esterHCID 15607334—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product2-Hydroxyethyl 5-norbornene-2-carboxylate t-butyl 5-norbornene-2-carboxylate 5-norbornene 2-carboxylic acid maleic anhydrideHCID 86593317—

Reaction Steps

1 mole of maleic anhydride, 0.05-0.8 moles of 2-hydroxyethyl 5-norbornene-2-carboxylate, 0.5-0.95-moles of t-butyl 5-norbornene-2-carboxylate and 0.01 to 0.2 moles of 5-norbornene 2-carboxylic acid are dissolved in tetrahydrofuran or toluene. A radical reaction is executed at a temperature of about 60-70° C. for 4-24 hours under a nitrogen or argon atmosphere in the presence of 0.5-10 g of azobisisobutyronitrile (AIBN), as an initiator. The resin thus produced by this polymerization is precipitated in ethyl ether or hexane and dried to yield poly [2-hydroxyethyl 5-norbornene-2-carboxylate/t-butyl 5-norbornene-2-carboxylate/5-norbornene 2-carboxylic acid/maleic anhydride] resin of the following Formula X.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06808859B1
Source datasetuspto-grants-2004_10
ORD IDord-a20214efb94441a39a7f941f21d504a9
Source noteuspto-grants-2004_10