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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899502Generated: October 29, 2026

4-Iodophenol → Methyl 5-[(4-iodophenoxy)methyl]furan-2-carboxylate

https://huagongshe.com/reaction/899502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenolHCID 10894—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 5-(chloromethyl)-2-furoateHCID 75065—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-[(4-iodophenoxy)methyl]furan-2-carboxylateHCID 99760528%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of 4-iodophenol (10.08 g, 45.8 mmol) in N,N-dimethylformamide (30 mL) was added to a ice-bath cooled suspension of sodium hydride (60%; 1.65 g, 41.2 mmol) in N,N-dimethylformamide (30 mL). The ice bath was removed and the mixtrue was stirred for 1 h. The mixture was cooled again to ˜5° C. and a solution of 5-(chloro-methyl)-furan-2-carboxylic acid methyl ester (4.00 g, 22.9 mmol) in N,N-dimethylformamide (60 mL) was added. The reaction mixture was stirred overnight at room temperature, then the solvents were evaporated under reduced pressure and water was added. The mixture was extracted three times with ethyl acetate and the combined organic layers were washed twice with 1 M NaOH, and once each with water and brine. The organic solution was dried (magnesium sulfate), filtered, evaporated, and purified using a Biotage 65 L purification system, eluting with 3% methylene chloride/toluene to give 5-(4-iodo-phenoxymethyl)-furan-2-carboxylic acid methyl ester (2.3 g, 28%) as a white solid, along with some mixed fractions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07355049B2
Source datasetuspto-grants-2008_04
ORD IDord-75bac77903f548979f76432f914c9b26
Source noteuspto-grants-2008_04