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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | (Bromomethyl)cyclooctane | HCID 18459730 | — |
| Edukt | 1-Benzylspiro[indole-3,4'-piperidin]-2(1H)-one | HCID 49760220 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-Benzyl-5-(cyclooctyl-methyl)-spiro[indoline-3,4'-piperidin]-2-one | HCID 68538883 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07655670B2 |
|---|
| Quelldatensatz | uspto-grants-2010_02 |
|---|
| ORD ID | ord-b60e0c43a94048c782d121424baf754a |
|---|
| Quellennotiz | uspto-grants-2010_02 |
|---|