HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54286994, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Bromo-2,5-furandione | HCID 80027 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 53941239 | HCID 53941239 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54286994 | HCID 54286994 | — |
Reaction Steps
A mixture of sodium acetate (14.76 g, 180.0 mmol) and acetic anhydride (150 ml) is heated, under N2, to 120° for 10 min., and is then chilled to 10°. 2-Ethyl-2-propenal dimethylhydrazone (11.36 g, 90.0 mmol) is added, followed by addition of bromomaleic anhydride (16.41 g, 92.7 mmol) and the reaction mixture is stirred at 10° for ca. 1 hour. The mixture is then diluted with methylene chloride and filtered, and the solid is rinsed with methylene chloride until colorless. The filtrate is concentrated to remove the solvent and to give 1,4-dihydro-1-dimethylamino-5-ethyl-2,3-pyridine-dicarboxylic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05098466 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-563d4e2c1b494022b0fc9e8ad3c5d59e |
| Source note | uspto-grants-1992_03 |