HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235297Generated: October 31, 2026
Potassium Nitrate → HCID 178526422, compound
https://huagongshe.com/reaction/235297
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 178517030 | HCID 178517030 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 178526422 | HCID 178526422 | 81.5% |
Reaction Steps
The procedure of Cheesman, G. W. H., J. Chem. Soc. 1170 (1962), was adapted. To a stirred suspension of 5-bromo-2-hydroxybenzimidazole (105 mg, 0.49 mmol) in concentrated H2SO4 (1 mL) at 0° C. for 30 min was added KNO3 (58.5 mg, 0.58 mmol, Baker) in one portion. The mixture was stirred at 0° C. for 3 h then at room temperature for one day. The mixture became a red solution. Then it was poured into ice (30 g) resulting in the separation of a brown precipitate, which was collected by filtration and washed with distilled water (2×1 mL) followed by ethanol (2×1 mL) to give 141 mg of crude title compound (contains minor impurities by NMR). Crystallization from DMSO/H2O gave 103 mg of pure title compound (80.5%) as bright yellow needles: mp 290°-4° C. (dec.), changed color from 200° C. IR (KBr, cm-1): 3406, 3181, 1712, 1537. 1H NMR (DMSO-d6): δ 7.244 (s, 1H), 7.558 (s, 1H), 11.227 (s, 1H), 11.321 (s, 1H). HRMS: calcd for C7H4N3O3Br (M+) m/z 256.9433; found: 256.9439.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597922 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-3029c33867604509aedf02287fc34dff |
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| Source note | uspto-grants-1997_01 |
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