HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → 4-Benzoyl-2-nitrophenylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Chloro-3-nitrobenzophenone | HCID 41743 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Benzoyl-2-nitrophenylhydrazine | HCID 19858128 | 75% |
Reaction Steps
20 ml of hydrazine hydrate were added to the suspension of 52.33 g of 4-chloro-3-nitrobenzophenone in 200 ml of abs. ethanol under stirring. The reaction mixture was stirred at room temperature for 75 minutes, then slowly heated to the boiling point. After completion of the violent reaction, the mixture was refluxed for an additional 1 hour. After cooling down, the crystals were filtered by suction, thoroughly washed with water and dried at 80° C. Thus, 38.62 g (75%) of 4-benzoyl-2-nitrophenylhydrazine were obtained as orange-red crystals, m.p.: 163°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04916149 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-61633c24326744f5aeb3a541f73adf4b |
| Source note | uspto-grants-1990_04 |