HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588379Generated: October 25, 2026
Sulfuric Acid → 5-(4-iodo-1-methyl-1H-pyrazol-5-yl)-2H-tetrazole
https://huagongshe.com/reaction/588379
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 4-Iodo-1-methyl-1H-pyrazole-5-carbonitrile | HCID 60136631 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-iodo-1-methyl-1H-pyrazol-5-yl)-2H-tetrazole | HCID 117652803 | 90.2% |
Reaction Steps
A reaction vessel was charged with DMF (1.225 L), Preparation 21, 4-iodo-1-methyl-1H-pyrazole-5-carbonitrile (175 g, 751 mmol), sodium azide (147 g, 2.25 mol), and ammonium chloride (121 g, 2.25 mol). H2O (525 mL) was added slowly to minimize exotherm. The reaction mixture was heated at 100° C. overnight. The reaction mixture was cooled to room temperature and poured into a mixture of H2O (2 L) and ice (1 kg). An aqueous solution of NaNO2 (600 mL, 120 g NaNO2, 20% by weight) was added followed by the slow addition of aqueous H2SO4 until the pH of the reaction mixture was 1. The precipitate was collected via filtration, washed with H2O and dried in vacuo to afford 5-(4-iodo-1-methyl-1H-pyrazol-5-yl)-2H-tetrazole as a colorless solid (187 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227956B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-f442852da50b44c0bbe2640aea6e9147 |
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| Source note | uspto-grants-2016_01 |
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