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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726046Generated: November 1, 2026

Iodine → HCID 178506570, compound

https://huagongshe.com/reaction/1726046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium ThiosulfateHCID 24477—
Reactant1-(5-(Benzyloxy)-1H-indazol-1-yl)ethan-1-oneHCID 22567249—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178506570HCID 178506570—

Reaction Steps

68.84 g of iodine and then 23 g of potassium hydroxide are added to a solution of 28.24 g of 1-(5-benzyloxyindazol-1-yl)ethanone in 620 ml of dimethylformamide. The reaction medium is stirred at ambient temperature for approximately 3 hours. 23 g of potassium hydroxide are added and the medium is stirred at ambient temperature for 48 hours. The medium is treated with 600 ml of a sodium thiosulfate solution (100 g of sodium thiosulfate in 250 ml of distilled water), 600 ml of distilled water and 1 liter of ethyl acetate. The medium is stirred for a few minutes and is then separated by settling out. The aqueous phase is extracted with 4×600 ml of ethyl acetate. The combined organic phases are washed with 1 liter of a saturated sodium chloride solution, and then dried over magnesium sulfate. The solvent is evaporated off under reduced pressure in a rotary evaporator. The reaction crude is taken up in dichloromethane, and the solid is filtered off and rinsed with dichloromethane and with ethyl ether. 20.8 g of 5-benzyloxy-3-iodo-1H-indazole are collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-3cce9192967b411c8ba3e6e319be65ab
Source noteuspto-grants-2009_02