Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Cyclopentadiene | HCID 7612 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 13444163 | HCID 13444163 | — |
Reaction Steps
To 0.6 Mol of acetic anhydride were added at 25° C. 0.163 Mol 90% HNO3 over 45 minutes. The mixture was stirred for an additional 20 minutes before 0.1 Mol cyclopentadiene was added over a 1 hour period, maintaining the temperature at 25° C. The reaction mixture was stirred for an additional hour before it was poured onto ice water and extracted with methylene chloride. An oily residue (120% weight yield) was obtained. An aliquot was purified via Kugelrohr distillation removing first acetic acid/acetic anhydride followed by the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04219660 |
|---|
| Source dataset | uspto-grants-1980_08 |
|---|
| ORD ID | ord-f82794b4bf8e4110b2fe8f3c5461b7e0 |
|---|
| Source note | uspto-grants-1980_08 |
|---|