Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178514644 | HCID 178514644 | — |
| Catalyst | Lithium Chloride | HCID 433294 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178418369 | HCID 178418369 | 91.7% |
Reaction Steps
A solution of benzonitrile (60.0 g, 581.9 mmol, 1.0 equiv) in DMF (anhydrous) (600 mL) was placed in a flask that had been purged and maintained with an inert atmosphere of nitrogen. Ammonium chloride (40.5 g, 757.2 mmol, 1.3 equiv) was added, followed by the addition of lithium chloride (2.0 g, 47.2 mmol, 0.1 equiv). To the mixture was added azidosodium (49.4 g, 756.8 mmol, 1.3 equiv). The resulting solution was stirred overnight, while maintaining the temperature at 100° C. The solids were filtered out and washed with EtOAc. The filtrates were combined and concentrated in vacuo. The residue was dissolved in a 10% NaOH aqueous solution (350 ml). The resulting solution was extracted with EtOAc (100 mL) and the aqueous layers were combined. The pH value of the solution was adjusted to 2 with concentrated HCl. The solids were filtered out and dried over reduced pressure to yield 5-phenyl-1H-tetrazole (78.0 g) as a white solid. ES m/z: [M+H]+ calcd for C7H6N4, 147.1; found 147.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481549B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-1d320bdd5545478cb9a4e533712c4892 |
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| Source note | uspto-grants-2013_07 |
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