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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84470생성일: 2026년 10월 24일

Potassium Carbonate → 4,5-Dihydrobenzo[b]thieno[2,3-d]oxepine

https://huagongshe.com/ko/reaction/84470

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-(2-(2-Iodophenoxy)ethyl)thiopheneHCID 64084785—
촉매Tetraethylammonium ChlorideHCID 5946—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4,5-Dihydrobenzo[b]thieno[2,3-d]oxepineHCID 57900155—

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-7923b99daeb74876aea1a1cb1e406144
출처 메모uspto-grants-2014_09