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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768013Generated: October 31, 2026

Imidazole → 3-(2-Iodoethyl)-1-benzothiophene

https://huagongshe.com/reaction/1768013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(Benzo[b]thiophen-3-yl)ethanolHCID 15852206—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Iodoethyl)-1-benzothiopheneHCID 23614437—

Reaction Steps

To a stirred solution of 2-(1-benzothiophene-3-yl)ethanol (890 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-(1-benzothiophene-3-yl)ethyl iodide, was obtained as brown liquid. Yield: 1.2 g (85%); 285 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235569B2
Source datasetuspto-grants-2007_06
ORD IDord-9b9fb70f09f442fd87a07663cd3825d1
Source noteuspto-grants-2007_06