HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazinecarboxaldehyde → HCID 20310377, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazinecarboxaldehyde | HCID 12229 | — |
| Reactant | 3-Chloro-5-(trifluoromethyl)benzaldehyde | HCID 3857033 | — |
| Reactant | HCID 20310379 | HCID 20310379 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 20310377 | HCID 20310377 | — |
Reaction Steps
As described in Example 35, 3-chloro-5-(trifluoromethyl)benzaldehyde is converted to 3-chloro-6-[3-chloro-5-(trifluoromethyl)phenyl]pyridazine. This compound is reacted with formylhydrazine in refluxing n-butanol 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-1e25b41548ad4e19942674e318651ba5 |
| Source note | uspto-grants-1978_09 |