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HRID 84469作成日:2026年10月24日

2-Iodophenol → 3-(2-(2-Iodophenoxy)ethyl)thiophene

https://huagongshe.com/reaction/84469

反応式

関与物質

役割名称HCID仕込み量
反応物2-IodophenolHCID 10784—
反応物Thiophene-3-ethanolHCID 83731—
反応物Diethyl azodicarboxylateHCID 5462977—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-(2-Iodophenoxy)ethyl)thiopheneHCID 64084785—

反応手順

To a stirred solution of 2-iodophenol (6.7 g, 30.6 mmol), 2-(3-thienyl)ethanol (3.57 g, 27.8 mol) and triphenylphosphene (8.00 g, 30.6 mmol) in THF, was slowly added a solution of DEAD (4.8 ml, 30.6 mmol). Reaction mixture was stirred at room temperature for 3 hours. Purification on silica gave 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene. A mixture of 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene (1.55 g, 4.69 mmol), palladium(II) acetate (105 mg, 0.47 mmol), potassium carbonate (3.2 g, 23.45 mmol), triphenylphosphene (246 mg, 0.94 mmol) and tetraethylammonium chloride (1.3 g, 4.69 mmol) in DMF was microwaved at 100° C. for 1 hour. The reaction was diluted with dichloromethane and filtered through celite. The filtrate was washed with water, dried (MgSO4), and concentrated in-vacuo. Purification on silica gave 4,5-dihydrobenzo[b]thieno[2,3-d]oxepine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846762B2
出典データセットuspto-grants-2014_09
ORD IDord-558fc451011e4d648d8c02d6fa52669b
出典メモuspto-grants-2014_09