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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2218805Erstellt: 26. Oktober 2026

Acetic Acid → 1-Butyl-4-(2-cyclooct-1-enylphenyl)piperazine

https://huagongshe.com/reaction/2218805

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktButanalHCID 261—
EduktSodium BicarbonateHCID 516892—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-(2-Cyclooct-1-enylphenyl)piperazineHCID 69218982—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-Butyl-4-(2-cyclooct-1-enylphenyl)piperazineHCID 6921826274,5%

Reaktionsschritte

To a solution of 1-(2-cyclooct-1-enylphenyl)piperazine (11 mg, 0.0407 mmol) produced in Example (46a) in tetrahydrofuran (1 mL) were added butyraldehyde (0.0047 mL, 0.0529 mmol), sodium triacetoxyborohydride (11.2 mg, 0.0529 mmol) and acetic acid (0.0044 mL, 0.0773 mmol), followed by stirring for 14 hours and 20 minutes at room temperature. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed three times with ethyl acetate. The organic layer was concentrated to produce a residue, which was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 9.9 mg of 1-butyl-4-(2-cyclooct-1-enylphenyl)piperazine as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07410971B2
Quelldatensatzuspto-grants-2008_08
ORD IDord-c60c9c39b75d4a1dbf0bf0ddaeee3081
Quellennotizuspto-grants-2008_08