Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029008Generated: October 31, 2026

Hydrochloric Acid → HCID 71253308, compound

https://huagongshe.com/reaction/1029008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
ReactantHCID 21822801HCID 21822801—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 71253308HCID 71253308—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sulfuric acid (7.67 mL, 144 mmol) was added to a solution of 2-(1H-indazol-1-yl)aniline (1.771 g, 8.46 mmol) in concentrated HCl (2.030 mL, 25.4 mmol) at 0° C. The solution was stirred and after cooling back to 0° C., sodium nitrite (0.584 g, 8.46 mmol) in water (3.5 mL) was added dropwise. The reaction was stirred 40 min at 0° C. before potassium iodide (2.81 g, 16.93 mmol) in water (3.5 mL) was added dropwise and the solution was stirred at RT. After 1 h, the reaction is poured into ice with ethyl acetate and separated. The aqueous layer was extracted with EtOAc. The combined organic extracts were washed with 1N HCl, water, saturated sodium bicarbonate, 1N sodium sulfite, and dried over sodium sulfate. The solution was filtered and concentrated in vacuo to give the crude material as an orange oil. The crude material was purified by silica gel chromatography by eluting with 1:4 EtOAc in hexane, to provide 1-(2-iodophenyl)-1H-indazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-3a6afc6d8c28483a9a538e9e67b94274
Source noteuspto-grants-2014_05