HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → Bicyclo[2.2.1]hept-5-ene-2-methanol bicyclo[2.2.1]hept-5-ene-2-carboxylic acid norbornene maleic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 2-Norbornene | HCID 10352 | — |
| Reactant | Bicyclo(2.2.1)hept-5-ene-2-methanol | HCID 78946 | — |
| Reactant | 5-Norbornene-2-carboxylic acid | HCID 78949 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Bicyclo[2.2.1]hept-5-ene-2-methanol bicyclo[2.2.1]hept-5-ene-2-carboxylic acid norbornene maleic anhydride | HCID 86759191 | — |
Reaction Steps
To 70 ml of tetrahydrofuran was added 0.04 M of norbornylene, 0.1 M of bicyclo[2.2.1]hept-5-ene-2-methanol, 0.06 M of bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 0.2 M of maleic anhydride and 0.4 g of AIBN. The resulting solution was reacted at 67° C. for 8 hours. Thereafter, a polymer was precipitated and filtered in petroleum ether/ether (1/1) solution, to obtain the title polymer. Here, the polymer was washed with aqueous Na2CO3 solution (5%), and re-washed with distilled water to completely remove base. The resulting resin was vacuum-dried to obtain a pure resin (yield: 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06630281B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-3da923555ce94d79bc6c6fa0db87a994 |
| Source note | uspto-grants-2003_10 |