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HRID 1178812作成日:2026年10月25日

Imidazole → 3-(2-Iodoethyl)-7-methoxy-1-benzofuran

https://huagongshe.com/reaction/1178812

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物IodineHCID 807—
反応物TriphenylphosphineHCID 11776—
反応物3-(2-Hydroxyethyl)-7-methoxybenzofuranHCID 22662935—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-Iodoethyl)-7-methoxy-1-benzofuranHCID 23614447—

反応手順

To a stirred solution of 2-(7-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 mixture 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-(7-methoxy-1-benzofuran-3-yl)ethyl iodide, was obtained as a brown liquid. Yield: 1.3 g (86%); (M+H): 302.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07276603B2
出典データセットuspto-grants-2007_10
ORD IDord-f46e7d2007a84caf9d6ae20234802835
出典メモuspto-grants-2007_10