HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzaldehyde → HCID 593142, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Chloro-6-hydrazinopyridazine | HCID 100787 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 593142 | HCID 593142 | 91.5% |
Reaction Steps
A mixture of 14.5 g (0.1 moles) of 6-chloro-3-pyridazinylhydrazine, 145 ml of ethanol and 15.1 g (0.1 moles) of 4-nitrobenzaldehyde is refluxed with stirring for 2 hours, cooled and 75 ml of water are added. The precipitate is filtered, washed with water, triturated with hot ethanol, filtered again and dried to give 25.4 g (91.5%) of the named compound; m.p. 290° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04329457 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-9cc2d0264dd140b992a32a6608405655 |
| Source note | uspto-grants-1982_05 |