HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → t-Butyl maleimide t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 2-hydroxyethyl 5-norbornene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 2-Hydroxyethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate | HCID 12033823 | — |
| Reactant | 1H-Pyrrole-2,5-dione, 3-(1,1-dimethylethyl)- | HCID 12229417 | — |
| Reactant | t-Butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate | HCID 18413667 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | t-Butyl maleimide t-butyl bicyclo[2,2,2]oct-5-ene-2-carboxylate 2-hydroxyethyl 5-norbornene-2-carboxylate | HCID 86756648 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06225020B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-72426b4d5d1e41fbb872ff127f53c17f |
| Source note | uspto-grants-2001_05 |