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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178817Generated: October 26, 2026

Imidazole → 3-(2-Iodoethyl)-5-methoxy-1-benzofuran

https://huagongshe.com/reaction/1178817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(5-Methoxy-1-benzofuran-3-yl)ethanolHCID 14982873—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Iodoethyl)-5-methoxy-1-benzofuranHCID 23614442—

Reaction Steps

To a stirred solution of 2-(5-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. It was then extracted with chloroform, washed well with 5% Na2S2O3 and the organic layer 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, 2-(5-methoxy-1-benzofuran-3-yl)ethyl iodide, was obtained as a brown liquid. Yield: 1.1 g (73%); (M+H): 302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276603B2
Source datasetuspto-grants-2007_10
ORD IDord-d98cbe5b2ddc462bb5ae73e2d9789a86
Source noteuspto-grants-2007_10