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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1441673Erstellt: 25. Oktober 2026

Potassium Iodide → 1-Benzyl-5-(cyclooctyl-methyl)-spiro[indoline-3,4'-piperidin]-2-one

https://huagongshe.com/reaction/1441673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt(Bromomethyl)cyclooctaneHCID 18459730—
Edukt1-Benzylspiro[indole-3,4'-piperidin]-2(1H)-oneHCID 49760220—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Benzyl-5-(cyclooctyl-methyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 68538883—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

1-Bromomethyl-cyclooctane (0.087 g, 0.424 mmol) and 1-benzyl-spiro[indoline-3,4′-piperidin]-2-one (0.030 g, 0.141 mmol) were dissolved in dry N,N-dimethylformamide (3 mL). Potassium carbonate (0.078 g, 0.565 mmol) and a catalytic amount of potassium iodide were added. The reaction mixture was then stirred at 55° C. under nitrogen atmosphere for 18 hours. The reaction mixture was partitioned with water and ethyl acetate. The organic layer was washed with brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield a crude oil. The crude oil was purified via flash chromatography (50% ethyl acetate/hexanes) to yield the title compound as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07655670B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-b60e0c43a94048c782d121424baf754a
Quellennotizuspto-grants-2010_02