HuagongsheHuagongshe Chemistry Print Report · For research reference only
Maleic Anhydride → 2-Hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate t-butyl 5-norbornene-2-carboxylate maleic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 1,1-dimethylethyl ester | HCID 15607334 | — |
| Reactant | 2-Hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate | HCID 70179192 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate t-butyl 5-norbornene-2-carboxylate maleic anhydride | HCID 86758320 | 89.5% |
Reaction Steps
2-hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate (0.15 mol), t-butyl 5-norbornene-2-carboxylate (0.85 mol), and maleic anhydride (1 mol) were dissolved in a tetrahydrofuran solvent. 2,2-azobisisobutyonitrile (5.84 g) was added, and the solution was mixed. The solution was polymerized at a temperature of 67° C. in a nitrogen atmosphere for 10 hours. After the polymerization reaction was completed, the polymer was precipitated in an ethyl ether solvent, then dried in a vacuum to obtain the pure title polymer (63.94 g). (yield: 22%, purity: 99.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06416926B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-4fd7717d03774bdf8be00243ec5b75de |
| Source note | uspto-grants-2002_07 |