HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 19081402, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | HCID 178448755 | HCID 178448755 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19081402 | HCID 19081402 | 74.9% |
Reaction Steps
50 ml of a dry benzene solution of 3.1 g of 5-amino-2-tert-butyl-4-hydroxypyridazin-3-(2H)-one, 1.9 g of isonicotinaldehyde and 0.17 g of p-toluene sulfonic acid, was reacted for 1.5 hours under heating and refluxing by means of a Dean Stark trap. After cooling, 100 ml of ethyl acetate was added to the reaction mixture, and the mixture was washed with water and then with a saturated sodium chloride aqueous solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 3.3 g of 2-tert-butyl-4-hydroxy-5-(4-pyridylimino)pyridazin-3-(2H)-one as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763439 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-c4567f0329c34b74bbfb70c81ded8744 |
| Source note | uspto-grants-1998_06 |