HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → N-ethyl-3,6-diformylcarbazole bis(N-phenylhydrazone)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | 9-ethyl-9H-carbazole-3,6-dicarbaldehyde | HCID 3716675 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-ethyl-3,6-diformylcarbazole bis(N-phenylhydrazone) | HCID 69210930 | — |
Reaction Steps
Phenylhydrazine (0.2 mole, commercially available from Aldrich, Milwaukee, Wis.) and N-ethyl-3,6-diformylcarbazole (0.1 mole) were dissolved in 100 ml of a 1:1 v/v mixture of toluene and THF in 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 N-ethyl-3,6-diformylcarbazole bis(N-phenylhydrazone) crystals formed upon standing were filtered off, washed with isopropanol and dried in a vacuum oven at 50° C. for 6 hours. Without further purification, the product was used for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179574B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-a579947bca0647aaace9a377a5b0c050 |
| Source note | uspto-grants-2007_02 |