HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-(Trifluoromethyl)phenyl)hydrazine → 4,5-Dibromo-2-[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-(Trifluoromethyl)phenyl)hydrazine | HCID 98650 | — |
| Reactant | Mucobromic Acid | HCID 3033972 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,5-Dibromo-2-[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-one | HCID 16779301 | 68.9% |
Reaction Steps
A solution of 21.4 grams of mucobromic acid and 13.3 grams of 3-trifluoromethylphenyl hydrazine in 60 milliliters of ethanol was stirred for about 10 minutes. The ethanol was removed by evaporation under reduced pressure, and then 40 milliliters each of glacial acetic acid and acetic anhydride were added to the reaction vessel. The acidic reaction mixture was heated at reflux for 4 hours. The reaction solvent was removed by evaporation under reduced pressure whereupon a solid precipitate formed. The solid was purified by recrystallization from ethanol. A yield of 20.7 grams of 1-(3-trifluoromethylphenyl)-4,5-dibromo-1,6-dihydro-6-oxopyridazine was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04366155 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-4912cb79dc0b4c9dbcf5dc2e40300929 |
| Source note | uspto-grants-1982_12 |