HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614809Generated: October 29, 2026
3-Nitrosalicylic acid → HCID 178522675, compound
https://huagongshe.com/reaction/614809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Nitrosalicylic acid | HCID 6807 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | HCID 178509299 | HCID 178509299 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178522675 | HCID 178522675 | 22.9% |
Reaction Steps
Anhydrous 5-aminotetrazole (15 g) and phosphorus trichloride (6 ml) were added to a suspension of 3-nitrosalicylic acid (16 g) in dry benzene (250 ml). The mixture was stirred and heated at reflux for 20 hours. The mixture was then cooled and diluted with petroleum ether (b.p. 60°-80° C.; 250 ml) and the resulting solid was filtered off. The solid was treated with dilute hydrochloric acid (200 ml; 2N) and the mixture was stirred for 30 minutes, and the solid was then filtered off and washed with ethanol and dissolved in aqueous ammonia solution (2N). This solution was treated with decolourizing charcoal and filtered and the filtrate was acidified by treatment with concentrated hydrochloric acid to give 2-hydroxy-3-nitro-N-(tetrazol-5-yl)benzamide (5.0 g), m.p. 236°-238° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04146631 |
|---|
| Source dataset | uspto-grants-1979_03 |
|---|
| ORD ID | ord-a9dcdf6196424e3e89bfe337c9b1ab7f |
|---|
| Source note | uspto-grants-1979_03 |
|---|