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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615348Generated: October 31, 2026

Iodine → HCID 178519380, compound

https://huagongshe.com/reaction/1615348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium DithioniteHCID 24489—
ReactantSodium BisulfateHCID 516919—
Reactant1H-Indazole-5-carboxaldehydeHCID 21250644—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178519380HCID 17851938035%

Reaction Steps

To a solution of 1H-indazole-5-carbaldehyde (315.2 mg, 2.16 mmol), K2CO3 (598.8 mg, 4.33 mmol) in DMF (2.5 mL) was added dropwise a solution of I2 (938 mg, 3.7 mmol) in DMF (2.5 mL) and the reaction allowed to stir for three hours. An aqueous solution consisting of Na2S2O4 (511 mg)/K2CO3 (35 mg)/H2O (3.5 mL) was then added and the solution stirred for two hours. Water (30 mL) and aqueous sodium hydrogen sulfate (1M, 10 mL) was added and the product was extracted with ethyl acetate (350 mL); this organic layer was washed with brine (3×25 mL). The aqueous layer was then extracted with dichloromethane (3×75 mL), this second organic layer was also washed with brine (25 mL). TLC indicated product present in both, so the residues were combined and purified by chromatography (10 g silica SPE tube, Silicycle, 5% ethyl acetate in dichloromethane) to yield a beige solid (203 mg, 35%). A precipitate that formed in the original aqueous layer was collected by vacuum filtration to give after drying a beige solid (first crop 135.6 mg, 23%; second crop 147 mg, 25%). 1H NMR (400 MHz, CDCl3 plus a drop of CD3OD) δ 10.03 (s, 1H), 8.00 (s, 1H), 7.95 (d, J=8.8 Hz, 1H), 7.54 (d, J=8.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765748B2
Source datasetuspto-grants-2014_07
ORD IDord-65f307fb2b87442e9f3a59361b5c7153
Source noteuspto-grants-2014_07