HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 178525021, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Benzyl 2-benzyloxy-5-cyanobenzoate | HCID 18974028 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178525021 | HCID 178525021 | 101.9% |
Reaction Steps
A solution of 436 mg (1.27 mmol) of benzyl 2-benzyloxy-5-cyanobenzoate, 91 mg (1.40 mmol) of sodium azide, and 68 mg (1.27 mmol) of ammonium chloride in 5 mL of DMF is heated at 120° C. for 24 hrs. The DMF was removed by rotoevaporation, the residue is taken up in water, and acidified. The white precipitate is collected by filtration and dried to give 500 mg of unpurified benzyl 2-benzyloxy-5-(1H-tetrazol-5-yl)benzoate, which is treated with 28% aqueous ammonium hydroxide in 5 mL of MeOH at 85° C. for 72 hrs. The reaction mixture was concentrated, taken up in water, and then acidified. Filtration of the precipitate gives 400 mg (1.04 mmol, 82% yield) of 2-benzyloxy-5-(1H-tetrazol-5-yl)benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08110570B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-dc3f10dcd0af4f3da12dd460bb2199b3 |
| Source note | uspto-grants-2012_02 |