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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128891생성일: 2026년 10월 26일

Ethyl Acetate → 1-(3-Iodophenoxy)-3,6,9-trioxadecane

https://huagongshe.com/reaction/128891

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물3-IodophenolHCID 12272—
반응물2-(2-(2-Methoxyethoxy)ethoxy)ethyl methanesulfonateHCID 12621272—
용매DimethylformamideHCID 6228—
용매HexaneHCID 8058—
생성물1-(3-Iodophenoxy)-3,6,9-trioxadecaneHCID 1898700361.6%

반응 조건

온도68 °C

반응 단계

To a solution of 1-[(methanesulfonyl)-oxy]-3,6,9-trioxadecane (11.6 g, 47.9 mmol) in dry DMF (145 ml) was added 3-iodophenol (10.6 g, 48.2 mmol) and potassium carbonate (6.6 g, 47.8 mmol). The reaction was immersed in an oil bath which was warmed to 68° C. over a period of 0.5 hr. The reaction was stirred at this temperature under an N2 atmosphere for 16 hrs and then at 82° C. for an additional 2 hrs. At the end of this period, the reaction was cooled, diluted with DMF, filtered through a pad of celite and evaporated in vacuo. The resulting residue was taken up into ethyl acetate (500 ml), washed with water (200 ml), 1N aqueous sodium hydroxide (200 ml) and brine (200 ml), dried (Na2SO4), filtered and evaporated in vacuo to provide a light brown oil. Flash column chromatography (silica, 1:3 to 1:2; EtOAc:hexane) provided 1 -(3-iodophenoxy)-3,6,9-trioxadecane as a light yellow oil (10.8 g, 37.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05466435
출처 데이터셋uspto-grants-1995_11
ORD IDord-7e492b043bfe4ec695a995ef1030b663
출처 메모uspto-grants-1995_11