HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobenzaldehyde → n'((4-Bromophenyl)methylidene)-3-phenyl-1h-indole-2-carbohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | 3-phenyl-1H-indole-2-carbohydrazide | HCID 2763658 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | n'((4-Bromophenyl)methylidene)-3-phenyl-1h-indole-2-carbohydrazide | HCID 70129263 | — |
Reaction Steps
A solution of Example 1C (1.76 g, 7.0 mmol) and 4-bromobenzaldehyde (1.36 g, 7.35 mmol) in ethanol (120 mL) was refluxed for 18 hours, cooled to room temperature, and filtered. The resulting solid was washed with ethanol and dried under vacuum to provide
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323228B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-d621275b2cec4254b59c576f3b348f34 |
| Source note | uspto-grants-2001_11 |