HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzonitrile → 4-(4-Cyanophenyl)amino-2,6-dimethyl-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | 4-Chloro-2,6-dimethyl-3-nitropyridine | HCID 10702725 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-Cyanophenyl)amino-2,6-dimethyl-3-nitropyridine | HCID 10611943 | — |
Reaction Steps
A solution of 4-chloro-2,6-dimethyl-3-nitropyridine (9.80 g, 52.5 mmol) and 4-aminobenzonitrile (6.20 g, 52.5 mmol) in ethanol (160 ml) was stirred at room temperature for 16 hours. The solvent was removed under reduced pressure and the residue was dissolved in dichloromethane (200 ml), and washed with saturated aqueous sodium bicarbonate (100 ml). The organic phase was dried (MgSO4) and concentrated under reduced pressure to give a gum which was crystallised by adding ether (100 ml) and sonicating for 5 minutes. The yellow solid (9.80 g, 70%) was filtered off and dried in vacuo, mp 171°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120747 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-975684f4a4d3454c813050aacdfc93c0 |
| Source note | uspto-grants-1992_06 |