HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetohydrazide → HCID 20310378, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetohydrazide | HCID 14039 | — |
| Reactant | 2,3-Dichlorobenzaldehyde | HCID 35745 | — |
| Reactant | HCID 20310375 | HCID 20310375 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 20310378 | HCID 20310378 | — |
Reaction Steps
As described in Example 35, 2,3-dichlorobenzaldehyde is converted to 3-chloro-6-(2,3-dichlorophenyl)pyridazine. A mixture of this compound and acetic acid hydrazide in n-butanol is refluxed for 24 hours to give the product of the example.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04112095 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-d97dcd89852f4d509938fdd8ab47b775 |
| Source note | uspto-grants-1978_09 |