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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Acetonitrile | HCID 6342 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | (Bromomethyl)cyclooctane | HCID 18459730 | — |
| Edukt | 1-(Methylcarbonyloxy-ethyl)-spiro[indoline-3,4'-piperidin]-2-one | HCID 58878482 | — |
| Produkt | 1-(Methylcarbonyloxy-methyl)-5-(cyclooctyl-methyl)-spiro[indoline-3,4'-piperidin]-2-one | HCID 68537343 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07655670B2 |
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| Quelldatensatz | uspto-grants-2010_02 |
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| ORD ID | ord-839936d770ef41f1a7c8425a6ccf07e9 |
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| Quellennotiz | uspto-grants-2010_02 |
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