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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantSodium NitriteHCID 23668193—
Reactant4-Iodo-1-methyl-1H-pyrazole-5-carbonitrileHCID 60136631—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(4-iodo-1-methyl-1H-pyrazol-5-yl)-2H-tetrazoleHCID 11765280390.2%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227956B2
Source datasetuspto-grants-2016_01
ORD IDord-f442852da50b44c0bbe2640aea6e9147
Source noteuspto-grants-2016_01