HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → 4-(Diphenylamino) benzaldehyde phenylhydrazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(Diphenylamino) benzaldehyde phenylhydrazone | HCID 4169641 | — |
Reaction Steps
Phenylhydrazine (0.1 mole, commercially available from Aldrich, Milwaukee, Wis.) and 4-(Diphenylamino)benzaldehyde (0.1 mole, available from Fluka, Buchs SG, Switzerland) were dissolved in 100 ml of isopropanol in a 250 ml 3-neck round bottom flask equipped with a reflux condenser and a mechanical stirrer. The solution was refluxed for 2 hours. Thin layer chromatography indicated the disappearance of the starting materials. At the end of the reaction, the mixture was cooled to room temperature. The 4-(diphenylamino)benzaldehyde phenylhydrazone crystals that formed upon standing were filtered off and washed with isopropanol and dried in a vacuum oven at 50° C. for 6 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07090953B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-104ff321bab547fca24b0966005c6059 |
| Source note | uspto-grants-2006_08 |