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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84469생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/84469

반응식

참여 물질

역할이름HCID투입량
반응물2-IodophenolHCID 10784—
반응물Thiophene-3-ethanolHCID 83731—
반응물Diethyl azodicarboxylateHCID 5462977—
용매TetrahydrofuranHCID 8028—
생성물3-(2-(2-Iodophenoxy)ethyl)thiopheneHCID 64084785—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846762B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-558fc451011e4d648d8c02d6fa52669b
출처 메모uspto-grants-2014_09