HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432695Generated: October 26, 2026
Anthranilic Acid → 2-(5-methyl-1H-tetrazol-1-yl)benzoic acid
https://huagongshe.com/reaction/432695
Participants
| Role | Name | HCID | Charge |
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| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-(5-methyl-1H-tetrazol-1-yl)benzoic acid | HCID 12524192 | 87.6% |
Reaction Steps
Under a nitrogen atmosphere, a solution of 2-aminobenzoic acid (100.0 g, 0.73 mol) in acetic anhydride (400 ml, 4.2 mol) was heated to reflux for 2 hours. The reaction was cooled to room temperature and the solvent was removed in vacuo. The residue was dissolved in glacial acetic acid (500 ml) and NaN3 (49.77 g, 0.77 mol) was added. The mixture was stirred overnight at room temperature followed by concentration of the acetic acid in vacuo. The residue was dissolved in 10% NaOH (500 ml) solution and heated to reflux for 3.5 hours. The reaction was cooled to room temperature and then poured over a mixture of ice water (2 L) and HCl (150 ml). A white solid precipitated and was collected by vacuum filtration. The solid was dried in vacuo to yield 130.5 g of 2-(5-methyl-1H-tetrazol-1-yl)benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06664260B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-039aaed079db4a71879948c858bc0d63 |
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| Source note | uspto-grants-2003_12 |
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