HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentadiene → 826-62-0
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentadiene | HCID 7612 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Product | 826-62-0 | HCID 13223 | — |
Reaction Steps
Using the procedure of Example 1, cyclopentadiene was reacted with maleic anhydride to provide 5-norbornene-2,3-dicarboxylic anhydride, which was then slowly added to a 10% NaOH aqueous solution. The resulting mixture was heated to about 85° C. for about 90 minutes and slowly cooled to room temperature. The resulting solution was neutralized by adding 10% sulfuric acid drop-wise. The reaction mixture was extracted using ethyl acetate. The organic phase was separated, dried over anhydrous MgSO4, filtered, and concentrated to yield 5-norbornene-2,3-dicarboxylic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06426171B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-f5060602e17a4317af4354b934b90018 |
| Source note | uspto-grants-2002_07 |