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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1441671Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1441671

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktAcetonitrileHCID 6342—
EduktPotassium CarbonateHCID 11430—
Edukt(Bromomethyl)cyclooctaneHCID 18459730—
Edukt1-(Methylcarbonyloxy-ethyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 58878482—
Produkt1-(Methylcarbonyloxy-methyl)-5-(cyclooctyl-methyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 68537343—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

1-Bromomethyl-cyclooctane (0.026 g, 0.216 mmol) and 1-(methylcarbonyloxy-ethyl)-spiro[indoline-3,4′-piperidin]-2-one (0.029 g, 0.105 mmol) were dissolved in acetonitrile (1.5 mL). Potassium carbonate (0.044 g, 0.316 mmol) and a catalytic amount of potassium iodide were added and the reaction mixture was stirred at 45° C. under nitrogen atmosphere for 18 hours. The reaction mixture was then 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 (3% methanol/dichloromethane) to yield the title compound as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07655670B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-839936d770ef41f1a7c8425a6ccf07e9
Quellennotizuspto-grants-2010_02