HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzaldehyde → HCID 178437938, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | HCID 178437963 | HCID 178437963 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178437938 | HCID 178437938 | — |
Reaction Steps
0.61 g (4 mmol) of p-nitrobenzaldehyde is added to a solution of 1.19 g (4 mmol) of 3-amino-1-[[p-(dimethylamino)benzylidene]amino]-2-ethylimidazolium chloride in 10 ml of glacial acetic acid, the mixture is stirred at room temperature for 16 hours and the product is precipitated by the addition of ether. The product is then filtered off and recrystallized from ethanol. There is obtained 1-[[p-(dimethylamino)benzylidene]amino]-2-ethyl-3-[(p-nitrobenzylidene)amino]imidazolium chloride of melting point 250°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831151 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-00adb1d63c7840f798f465e5b8a149c1 |
| Source note | uspto-grants-1989_05 |