HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → Ethyl nitroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | Ethyl nitroacetate | HCID 69379 | — |
Reaction Steps
Another route was disclosed by early researchers Bouveault and Wahl, Bull. Soc. Chim. France, 31, 847-54 (1904), whereby ethyl acetoacetate was reacted with absolute nitric acid in acetic anhydride at 30°-35° C., but low yields of ethyl nitroacetate were reported. This work was later confirmed by Arndt and Rose in J. Chem. Soc. 1935, 1-10. The major product produced using the conditions of Bouveault and Wahl was found to be diethyl2-oxofurazan dicarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05162572 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-dab4f7c84a1646d0a19f1872afa404bf |
| Source note | uspto-grants-1992_11 |