HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895970Generated: October 30, 2026
Citraconic Anhydrides → 1,2-Dihydro-1-benzyl-4-methyl-3,6-pyridazinedione
https://huagongshe.com/reaction/895970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citraconic Anhydrides | HCID 12012 | — |
| Reactant | Benzylhydrazine dihydrochloride | HCID 146540 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,2-Dihydro-1-benzyl-4-methyl-3,6-pyridazinedione | HCID 561939 | — |
Reaction Steps
A slurry of citraconic anhydride (5.61 g, 50.0 mmol), benzylhydrazine dihydrochloride (9.80 g, 50.0 mmol) and potassium acetate (9.80 g, 100 mmol) in acetic acid (100 mL) was heated to reflux for 17 h. The reaction mixture was cooled and filtered. The filtrate was evaporated under reduced pressure and re-evaporated from toluene. The gummy yellow residue was partitioned between sodium carbonate solution (90 mL, 4 N) and EtOAc (50 mL). The aqueous extract was washed once with EtOAc and then slowly added to hydrochloric acid (3 M, 140 mL). The resulting white precipitate was collected, washed with water and dissolved in chloroform (1 L). The insoluble material was collected and boiled in EtOAc and filtered hot, to give 1,2-dihydro-1-benzyl-4-methyl-3,6-pyridazinedione as a white solid, mp >200° C. (1.85 g, 17%). Part IA compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06919323B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-4ec74c0dd53b4866bbd86624ad0e50fe |
|---|
| Source note | uspto-grants-2005_07 |
|---|