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HRID 1873386作成日:2026年10月27日

Water → 2-[4-(4-Propylcyclohexyl)phenyl]selenophene

https://huagongshe.com/reaction/1873386

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物2-IodoselenopheneHCID 142183—
反応物4-(trans-4-Propylcyclohexyl)phenylboronic AcidHCID 3104710—
触媒HCID 178418397HCID 178418397—
溶媒Toluene ethanolHCID 21863594—
生成物2-[4-(4-Propylcyclohexyl)phenyl]selenopheneHCID 59456296—

反応手順

A mixture 0111.0 g (41.1 mmol) of 2-iodoselenophene, 7.98 g (32.4 mmol) of 4-(4-propylcyclohexyl)phenylboronic acid, 3.70 g (3.20 mmol) of tetrakis(triphenylphosphine)palladium(0) and 60 ml of 2 N sodium carbonate soln. in 160 ml of toluene/ethanol (1:1) is heated under reflux for 22 h. After cooling, water is added, and the batch is extracted a number of times with MTBE. The combined organic phases are washed with water, 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:EtOAc=20:1). The further purification is carried out by recrystallisation from n-heptane; 2-[4-(4-propylcyclohexyl)phenyl]selenophene is obtained as a colourless 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-76e1073097df4d6c889c3db6f8abdc88
出典メモuspto-grants-2012_11