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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768000Generated: October 26, 2026

Imidazole → 5-Chloro-3-(2-iodoethyl)-1-benzofuran

https://huagongshe.com/reaction/1768000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(5-Chloro-1-benzofuran-3-yl)ethanolHCID 23614438—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-3-(2-iodoethyl)-1-benzofuranHCID 23614439—

Reaction Steps

To a stirred solution of 2-(5-chloro-1-benzofuran-3-yl)ethanol (980 mg, 5 mmol) in anhydrous THF (50 ml), triphenylphosphine (1.572 g, 6 mmol), iodine (1.518 g, 6 mmol) and imidazole (408 mg, 6 mmol) were added at room temperature. The reaction mixture was stirred at room temperature for 4 hrs and quenched with water. It was extracted with chloroform, washed well with 5% Na2S2O3 solution and the organic layer was dried over anhydrous MgSO4. It was filtered and concentrated. The residue was purified by silica-gel column chromatography by eluting it with 30% ethyl acetate:hexane. The product, namely 2-(5-chloro-1-benzofuran-3-yl)ethyl iodide, was obtained as brown liquid; Yield: 1.2 g (80%); 306 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235569B2
Source datasetuspto-grants-2007_06
ORD IDord-c7d53180e3684ee39b7b17e39419855e
Source noteuspto-grants-2007_06