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HRID 1873421作成日:2026年10月25日

Hydrochloric Acid → 4'-Propyl-4-selenophen-2-ylbicyclohexyl-4-ol

https://huagongshe.com/reaction/1873421

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Ammonium ChlorideHCID 25517—
反応物SelenopheneHCID 136130—
反応物[1,1'-Bicyclohexyl]-4-one,4'-propyl-,HCID 4354185—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物4'-Propyl-4-selenophen-2-ylbicyclohexyl-4-olHCID 59456263—

反応条件

温度-50 °C

反応手順

25.0 g (0.19 mol) of selenophene are initially introduced in 250 ml of diethyl ether, and 130 ml (0.21 mol, 15% soln. in hexane) of n-BuLi are added. The mixture is warmed under reflux for 25 min and subsequently cooled to −50° C. A solution of 46.7 g (0.21 mol) of 4′-propylbicyclohexyl-4-one in 70 ml of diethyl ether is metered in, and the mixture is slowly warmed to RT. After 18 h, sat. ammonium chloride soln. and 2 N hydrochloric acid are added, and the organic phase is separated off. The aqueous phase is extracted with diethyl ether, and the combined organic phase is washed with 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=3:1→2:1). Further purification is carried out by recrystallisation from n-heptane. 4′-Propyl-4-selenophen-2-ylbicyclohexyl-4-ol is obtained as a yellow-brown 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-df76d5a1dcdc4ca2b1f9a2faca55b63e
出典メモuspto-grants-2012_11