HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitrobenzaldehyde → 4-[(2-Nitrophenyl)methylideneamino]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[(2-Nitrophenyl)methylideneamino]benzonitrile | HCID 616463 | 79.3% |
Reaction Steps
The mixture of 4-aminobenzonitrile (20 g, 0.17 mol) and 2-nitrobenzaldehyde (28.2 g, 0.17 mol) in anhydrous ethanol was heated to reflux for 3 h. The reaction mixture was cooled to room temperature. The solvent was removed under reduced pressure. The residue was washed with diethyl ether to give 4-(2-nitrobenzylideneamino)benzonitrile as yellow solid (33.7 g, yield 79.3%) LC/MS m/e obsd. (ESI+) [(M+H)+] 252.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546427B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-4e7a7291dd9c4b8c98ba6eb171ccb03d |
| Source note | uspto-grants-2013_10 |