HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amino-3-nitrobenzonitrile → 3,4-Diaminobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Amino-3-nitrobenzonitrile | HCID 595901 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,4-Diaminobenzonitrile | HCID 737285 | 90.1% |
Reaction Steps
A solution of 4-amino-3-nitrobenzonitrile (20 mmol) in MeOH (300 mL) in the presence of 5% of Pd/C (1 g) was treated with hydrogen at room temperature for 16 hours. The reaction mixture was filtered and concentrated to give 3,4-diaminobenzonitrile (2.4 g, 90% of yield), which was directly treated with formic acid (20 mL) under reflux for 4 hours. After removal of the excess formic acid, the residue was dissolved in EtOAc, washed with 10% sodium bicarbonate and brine, and dried over MgSO4. Concentration gave 5-cyanobenzimidazole (2.2 g, 85%). 1H NMR (CD3OD) δ8.39 (s, 1H), 8.05 (s, 1H), 7.76 (d, J=8.4 Hz, 1H), 7.59 (dd, J=8.4 Hz, J=1.1 Hz, 1H); MS: 144 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043257 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-1052122c2b4342b4919e71b81cca0d24 |
| Source note | uspto-grants-2000_03 |