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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429011Generated: October 30, 2026

Azobisisobutyronitrile → Maleic anhydride t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 3-hydroxypropyl 5-norbornene-2-carboxylate

https://huagongshe.com/reaction/429011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
Reactantt-Butyl bicyclo[2,2,2]oct-5-ene-2-carboxylateHCID 18413667—
SolventTetrahydrofuranHCID 8028—
ProductMaleic anhydride t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 3-hydroxypropyl 5-norbornene-2-carboxylateHCID 8675757850%

Reaction Steps

Maleic anhydride (1 mol.), t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate (0.5 mol.), and 3-hydroxy propyl 5-norbornene-2-carboxylate (0.5 mol.) were dissolved in 200 gms of tetrahydrofuran (THF), 6 gms of 2,2′-azobisisobutyronitrile (AIBN) was added thereto, and then the resultant solution was reacted at a temperature of 67° C. in a nitrogen atmosphere for 10 hours. After a high molecule weight was achieved by the reaction, the resultant product was precipitated in an ethyl ether solvent. The gathered precipitate was dried, and 150 gms of the desirable poly(maleic anhydride/t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate/3-hydroxypropyl 5-norbornene-2-carboxylate) polymer was obtained at a yield of about 50%. NMR spectra of the polymer is illustrated in FIG. 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316162B1
Source datasetuspto-grants-2001_11
ORD IDord-cf7fa89251d3477eb64d7e31765bd6fd
Source noteuspto-grants-2001_11