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HRID 1873394作成日:2026年10月27日

Sodium Carbonate → 2-(4-Ethoxy-2,3-difluorophenyl)selenophene

https://huagongshe.com/reaction/1873394

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2-BromoselenopheneHCID 137013—
反応物B-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
触媒HCID 178418397HCID 178418397—
溶媒Toluene ethanolHCID 21863594—
生成物2-(4-Ethoxy-2,3-difluorophenyl)selenopheneHCID 59456301—

反応手順

A mixture of 45.0 g (0.21 mol) of 2-bromoselenophene, 52.0 g (0.26 mol) of 4-ethoxy-2,3-difluorophenylboronic acid, 20.0 g (17.3 mmol) of tetrakis(triphenylphosphine)palladium(0) and 600 ml of 2 N sodium carbonate soln. in 1100 ml of toluene/ethanol (1:1) is heated under reflux for 20 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted with toluene. The combined organic phases are washed with sat. sodium hydrogencarbonate soln., 1 N hydrochloric acid and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:toluene=3:2). Further purification is carried out by recrystallisation from ethanol; 2-(4-ethoxy-2,3-difluorophenyl)selenophene is obtained as a beige solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304036B2
出典データセットuspto-grants-2012_11
ORD IDord-b0d75b2282834822b4ffc49a3ff86c7a
出典メモuspto-grants-2012_11