HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(4-Chlorobenzoyl)-2-(4-aminophenyl)hydrazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Barium Sulfate | HCID 24414 | — |
| Reactant | 4-Chlorobenzoic N2-(4-nitrophenyl)hydrazide | HCID 3106534 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Chlorobenzoyl)-2-(4-aminophenyl)hydrazine hydrochloride | HCID 21427826 | — |
Reaction Steps
1-(4-Chlorobenzoyl)-2-(4-nitrophenyl)hydrazine (2.92g, 0.01 mole) and 5% palladium or barium sulfate (catalytic amount) were suspended in a mixture of ethanol (350 ml) and concentrated hydrochloric acid (5 ml) in a Parr shaker bottle. The reaction mixture was hydrogenated at room temperature until the theoretical amount of hydrogen had been taken up. The reaction mixture was filtered and the solvent was evaporated from the filtrate leaving a tan solid. Yield 2.9 g (99%), m.p. 209° C (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04031127 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-44b258b34af04effa8513e253e8260b9 |
| Source note | uspto-grants-1977_06 |