HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975891Generated: October 26, 2026
Azobisisobutyronitrile → Ethyl maleimide t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 3-hydroxypropyl 5-norbornene-2-carboxylate
https://huagongshe.com/reaction/1975891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Ethyl maleimide | HCID 14671028 | — |
| Reactant | t-Butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate | HCID 18413667 | — |
| Reactant | 3-Hydroxypropyl 5-norbomene-2-carboxylate | HCID 23502028 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl maleimide t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 3-hydroxypropyl 5-norbornene-2-carboxylate | HCID 86756649 | 83% |
Reaction Steps
Ethyl maleimide (1 mol.), t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate (0.5 mol.) and 3-hydroxypropyl 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) was added thereto, and the resulting solution was reacted at a temperature between 60° C. and 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(ethyl maleimide/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 83%. NMR spectra of the polymer is illustrated in FIG. 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06225020B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-8075e20c3660497d8f10866387ef1c38 |
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| Source note | uspto-grants-2001_05 |
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