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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | t-Butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate | HCID 18413667 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Maleic anhydride t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 3-hydroxypropyl 5-norbornene-2-carboxylate | HCID 86757578 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316162B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-cf7fa89251d3477eb64d7e31765bd6fd |
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| Source note | uspto-grants-2001_11 |
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