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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178798Generated: October 25, 2026

Imidazole → 3-(2-Iodoethyl)-6-methoxy-1-benzofuran

https://huagongshe.com/reaction/1178798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(6-Methoxy-benzofuran-3-yl)ethanolHCID 23614444—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Iodoethyl)-6-methoxy-1-benzofuranHCID 23614445—

Reaction Steps

To a stirred solution of 2-(6-methoxy-1-benzofuran-3-yl)ethanol (960 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. The product was then extracted with chloroform, washed well with 5% Na2S2O3 solution and the organic layer dried over anhydrous MgSO4. It was then filtered and concentrated. The residue was purified by silica-gel column chromatography by eluting it with 30% ethyl acetate:hexane. The product, 2-(6-methoxy-1-benzofuran-3-yl)ethyl iodide, was obtained as a brown liquid. Yield: 1.2 g (80%); (M+H): 302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276603B2
Source datasetuspto-grants-2007_10
ORD IDord-e79d91c437494cf0b38f1624a56194a6
Source noteuspto-grants-2007_10