Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130657Generated: October 26, 2026

Iodine → 2-IODO-5-METHOXYPHENOL

https://huagongshe.com/reaction/130657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant3-MethoxyphenolHCID 9007—
CatalystSilver trifluoroacetateHCID 76299—
SolventChloroformHCID 6212—
Product2-IODO-5-METHOXYPHENOLHCID 1141401533.8%

Reaction Steps

I2 (40.9 g, 161.1 mmol) was dissolved in CHCl3 (850 mL) with stirring over 1 hour. The solution was added slowly into a reaction mixture of 3-methoxyphenol 5-A (20 g, 161.1 mmol) and silver trifluoroacetate in 200 mL CHCl3 over 1.5 hours. The reaction was stirred at room temperature for 16 hours. Solids were removed by filtration. The filtrate was washed with 5% Na2S2O3(500 mL), saturated NaHCO3, brine, dried over MgSO4 and concentrated. The crude mixture was triturated with carbon tetrachloride to give 2-iodo-5-methoxyphenol 5-B (13.6 g) as a white solid. The remaining crude products were purified by silica gel column chromatography eluted with CH2Cl2to give 28.2 g of compound 5-B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381824B2
Source datasetuspto-grants-2008_06
ORD IDord-b48948d38dc0418fa826935f20fc0fa1
Source noteuspto-grants-2008_06