HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → HCID 54221367, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,3-Cyclohexadiene | HCID 11605 | — |
| Product | HCID 54221367 | HCID 54221367 | — |
Reaction Steps
To 166 ml. of acetic anhydride were dropped 27.7 g. 20% nitric acid at 25° C. under ice cooling over a 45 minute period. This was followed by the hour long addition of 19.5 g. of 1,3-cyclo hexadiene at 25° C. (ice cooling from time to time). After an additional hour stirring the reaction was poured onto ice and worked up as above. Purification over silicagel yielded acetic acid (4-nitro-cyclohex-2-en-1-yl)ester as a cis/trans mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04079076 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-0a10ff2e43f04db9a10e5e1714727152 |
| Source note | uspto-grants-1978_03 |