HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzaldehyde → N-(4-Chlorophenyl)-3-nitrobenzenemethanimine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-Chlorophenyl)-3-nitrobenzenemethanimine | HCID 690813 | 92.1% |
Reaction Steps
A mixture of 4-chloro-phenylamine (6.4 g, 50 mmol) and 3-nitro-benzaldehyde (8.31 g, 55 mmol) in ethanol (100 mL) was prepared. The reaction mixture was heated to reflux for 3 h. Then the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford (4-chloro-phenyl)-(3-nitro-benzylidene)-amine (12 g, 92%) as a light yellow oil: LC/MS m/e calcd for C13H9ClN2O2 (M+H)+: 261.68, observed: 261.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344137B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-e4f8231d2f164f7bb64afb453833d6a1 |
| Source note | uspto-grants-2013_01 |