HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine Sulfate → 4-Bromopyridazine-3,6-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine Sulfate | HCID 24842 | — |
| Reactant | 3-Bromo-2,5-furandione | HCID 80027 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromopyridazine-3,6-diol | HCID 254942 | 151% |
Reaction Steps
This was prepared by a slight variation on the method of Kasnar et al., Nucleosides & Nucleotides, (1994), 13(1-3), 459-79. Hydrazine sulphate salt (51 g) was suspended in water (250 ml), heated to reflux and bromomaleic anhydride (90.38 g) was added dropwise. The mixture was heated at reflux for 4 h then cooled to room temperature. The reaction was repeated with 29 g hydrazine sulphate, 53 g bromomaleic anhydride and 130 ml water. The precipitates were collected by filtration, washed with water and acetone and dried as a combined batch in vacuo to afford 4-bromo-1,2-dihydro-3,6-pyridazinedione as a white solid (113 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709483B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-1064bbf706c646d0b6731344384145b0 |
| Source note | uspto-grants-2010_05 |