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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370269Erstellt: 25. Oktober 2026

Cyclooctanecarbaldehyde → N-[1-(cyclooctylmethyl)piperidin-4-yl]xanthene-9-carboxamide

https://huagongshe.com/reaction/370269

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclooctanecarbaldehydeHCID 81190—
EduktSodium BicarbonateHCID 516892—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktN-(piperidin-4-yl)xanthene-9-carboxamide hydrochlorideHCID 23283003—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-[1-(cyclooctylmethyl)piperidin-4-yl]xanthene-9-carboxamideHCID 1076519945,4%

Reaktionsschritte

1.16 g of N-(piperidin-4-yl)xanthene-9-carboxamide hydrochloride and 586 mg of cyclooctanecarbaldehyde were suspended in 60 ml of tetrahydrofuran at room temperature, and 1.60 g of sodium triacetoxyborohydride was added thereto, followed by stirring for 12 hours at the same temperature. Saturated aqueous sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, followed by drying over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (developing solvent: chloroform--chloroform/methanol=50/1), and 660 mg of the title compound as a white solid was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06140338
Quelldatensatzuspto-grants-2000_10
ORD IDord-9d8f9799d59b4fccaab715570a02b422
Quellennotizuspto-grants-2000_10