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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873421Erstellt: 23. Oktober 2026

Hydrochloric Acid → HCID 59456263, Verbindung

https://huagongshe.com/de/reaction/1873421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAmmonium ChlorideHCID 25517—
EduktSelenopheneHCID 136130—
Edukt[1,1'-Bicyclohexyl]-4-one,4'-propyl-,HCID 4354185—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 59456263HCID 59456263—

Reaktionsbedingungen

Temperatur-50 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304036B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-df76d5a1dcdc4ca2b1f9a2faca55b63e
Quellennotizuspto-grants-2012_11