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HRID 128891作成日:2026年10月26日

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

https://huagongshe.com/reaction/128891

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物3-IodophenolHCID 12272—
反応物2-(2-(2-Methoxyethoxy)ethoxy)ethyl methanesulfonateHCID 12621272—
溶媒DimethylformamideHCID 6228—
溶媒HexaneHCID 8058—
生成物1-(3-Iodophenoxy)-3,6,9-trioxadecaneHCID 1898700361.6%

反応条件

温度68 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05466435
出典データセットuspto-grants-1995_11
ORD IDord-7e492b043bfe4ec695a995ef1030b663
出典メモuspto-grants-1995_11