HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1007484Erstellt: 24. Oktober 2026
Ethyl Acetate → 3-Isopropyl-5-(4-nitro-2,6-dimethyl-phenoxy)-1H-indole
https://huagongshe.com/de/reaction/1007484
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Fluoro-1,3-dimethyl-5-nitrobenzene | HCID 11367232 | — |
| Edukt | 3-isopropyl-1H-indol-5-ol | HCID 22669491 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-Isopropyl-5-(4-nitro-2,6-dimethyl-phenoxy)-1H-indole | HCID 22669511 | — |
Reaktionsschritte
11.44 g (58.76 mmol) of 5-hydroxy-3-isopropyl-indole are dissolved in 350 ml of DMSO, 8.93 g (64.63 mmol) of potassium carbonate in solid form are introduced and subsequently 9.94 g (58.76 mmol) of 3,5-dimethyl-4-fluoronitrobenzene are added. The reaction solution is stirred for 2 hours at 100° C. under argon. Afterwards it is cooled to room temperature, 100 ml of ethyl acetate and 600 ml of H2O are added; ethyl acetate is separated off after phase separation and the aqueous phase is reextracted twice with ethyl acetate. The combined organic phases are washed twice with sodium chloride solution, dried over sodium sulphate, filtered and concentrated to dryness. The residue is purified by chromatography on silica gel by means of cyclohexane/ethyl acetate (10:1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06794406B2 |
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| Quelldatensatz | uspto-grants-2004_09 |
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| ORD ID | ord-c65647b50728423e988ab1d275144b03 |
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| Quellennotiz | uspto-grants-2004_09 |
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