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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465763Generated: November 2, 2026

N-Iodosuccinimide → 5-(2-hydroxyethyl)-6-iodo-2-benzofuran-1(3H)-one

https://huagongshe.com/reaction/1465763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant5-(2-hydroxyethyl)-2-benzofuran-1(3H)-oneHCID 66643961—
SolventTrifluoromethanesulfonic acidHCID 62406—
Product5-(2-hydroxyethyl)-6-iodo-2-benzofuran-1(3H)-oneHCID 66643870—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of 5-(2-hydroxyethyl)-2-benzofuran-1(3H)-one (9.00 g, 50.6 mmol) in 100 mL of TfOH was added NIS (12.5 g, 55.6 mmol), then the mixture was stirred at 0° C. for 2 hrs and then poured into ice-water (500 mL). The solution was extracted three times with 500 mL of EtOAc and the combined organic layers were washed with saturated NaHCO3 and brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by column chromatography (EtOAc/Pet Ether=1:5) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999991B2
Source datasetuspto-grants-2015_04
ORD IDord-3c59f644a3b14b9ab1588816e9bfc91a
Source noteuspto-grants-2015_04