Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624311Generated: October 30, 2026

Iodine → HCID 86691622, compound

https://huagongshe.com/reaction/624311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthylenediamineHCID 3301—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 71743951HCID 71743951—
Solventtert-ButanolHCID 6386—
ProductHCID 86691622HCID 8669162252%

Reaction Steps

A mixture of 5-chloro-4-fluoro-2-(4-fluorophenyl)benzofuran-3-carbaldehyde (1.2 g, 4.10 mmol) and ethylenediamine (0.277 m, 4.10 mmol) in t-BuOH (15 ml) under a N2 atmosphere in a 50 ml RB flask was stirred at room temperature for 30 minutes. Potassium carbonate (0.567 g, 4.10 mmol) followed by iodine (1.041 g, 4.10 mmol) were then added and the reaction mixture was heated at 70° C. for 2 hours. The solvent was removed and the residue diluted with ethyl acetate. The mixture was washed with 10% sodium thiosulfate solution. The organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified by using combiflash silica column using 8% methanol in chloroform as an eluent. The desired fractions were collected and concentrated to give the titled product (0.7 g, 52%). 1H NMR (400 MHz, CDCl3): δ 7.77-7.75 (m, 2H), 7.37-7.34 (m, 1H), 7.27-7.16 (m, 3H), 3.90 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303020B2
Source datasetuspto-grants-2016_04
ORD IDord-69e2d26a34c647759db237b795bdc381
Source noteuspto-grants-2016_04