HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 922443Erstellt: 25. Oktober 2026
Potassium Iodide → 6-(3-Methoxypropoxy)indan-1-one
https://huagongshe.com/reaction/922443
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 6-Hydroxy-1-indanone | HCID 7020659 | — |
| Edukt | Toluene-4-sulfonic acid 4-methoxy-butyl ester | HCID 86601716 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 6-(3-Methoxypropoxy)indan-1-one | HCID 68309939 | 50% |
Reaktionsschritte
To a solution of 6-hydroxyindan-1-one (1.48 g) in acetonitrile (30 mL) were added 4-methoxybutyl 4-methylbenzenesulfonate (2.93 g), potassium iodide (166 mg) and potassium carbonate (2.07 g), and the mixture was heated to stir at 80° C. for 5 hours. To the reaction mixture was added water under ice-cooling, and then the mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=7/3), and then triturated with n-hexane/isopropyl ether (2:1) to give 6-(3-methoxypropoxy)indan-1-one [REx(11-1)] (1.1 g) as a colorless powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09278944B2 |
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| Quelldatensatz | uspto-grants-2016_03 |
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| ORD ID | ord-c11c7a90bafb412ab0c1ba6aabc79425 |
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| Quellennotiz | uspto-grants-2016_03 |
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