HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzonitrile → 4-(1H-tetrazol-5-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(1H-tetrazol-5-yl)aniline | HCID 1079216 | — |
Reaction Conditions
| Temperature | 125 °C |
|---|
Reaction Steps
A mixture of 4-aminobenzonitrile (10 g, 84.6 mmol), sodium azide (16.5 g, 254 mmol) and ammonium chloride (13.6 g, 254 mmol) in DMF was heated at 125° C. for 16 hours. The cooled mixture was filtered and the filtrate was concentrated in vacuo. The residue was added water (200 mL) and diethyl ether (200 mL) which resulted in crystallisation. The mixture was filtered and the solid was dried in vacuo at 40° C. for 16 hours to afford 5-(4-aminophenyl)-2H-tetrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879893B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-6bf267942e8943dbb913b10e35ced7fb |
| Source note | uspto-grants-2011_02 |