Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351542Erstellt: 26. Oktober 2026

Water → HCID 178468978, Verbindung

https://huagongshe.com/reaction/351542

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt(1,1'-Bicyclohexyl)-4-oneHCID 41690—
EduktEthyl 4-(piperazin-1-yl)benzoateHCID 2761178—
EduktSodium cyanoborohydrideHCID 5003444—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelEthanolHCID 702—
ProduktHCID 178468978HCID 17846897820,3%

Reaktionsschritte

A mixture of 4-cyclohexylcyclohexanone (1.54 g), 1-(4-ethoxycarbonylphenyl)piperazine (2 g) and titanium(IV) isopropoxide (3.18 ml) was stirred at room temperature. After 1 hour, the IR spectrum of the mixture showed no ketone band, and the viscous solution was diluted with absolute ethanol (8.5 ml). Sodium cyanoborohydride (0.343 g) was added, and the solution was stirred for 3 hours. Water (3 ml) was added with stirring, and the resulting in organic precipitate was filtered and washed with ethanol. The filtrate was extracted with ethyl acetate. The organic layer was taken and dried over magnesium sulfate. The magnesium sulfate was filtered off, and filtrate was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel and eluted with (hexane/ethyl acetate)=(3/1). The fractions containing the less polar compound were collected and evaporated under reduced pressure to give ethyl 4-[4-(cis-4-cyclohexylcyclohexyl)piperazin-1-yl]benzoate (692 mg) as byproduct. The fractions containing the more polar compound were collected and evaporated under reduced pressure to give ethyl 4-[4-(trans-4-cyclohexylcyclohexyl)piperazin-1-yl]benzoate (587 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743776B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-9d9de2240edd40cca52a14699746cbfa
Quellennotizuspto-grants-2004_06