HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241619Erstellt: 25. Oktober 2026
Indole → 1-(4-methoxyphenyl)-3-(methylthio)-1H-indole
https://huagongshe.com/reaction/241619
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Indole | HCID 798 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Magnesium Bromide | HCID 82241 | — |
| Edukt | 1-(4-methoxyphenyl)-1H-indole | HCID 775715 | — |
| Edukt | 2-(Methylthio)isoindoline-1,3-dione | HCID 4101460 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 1-(4-methoxyphenyl)-3-(methylthio)-1H-indole | HCID 58378235 | 80% |
Reaktionsschritte
1-(4-methoxyphenyl)-1H-indole (synthesised from indole by an arylation process analogous to that described in step (a) of Example 1 [arylation process also described in J. Org. Chem. 2008, 73 (14), 5529-5535], 1.0 g, 4.48 mmol), 2-(methylthio)isoindoline-1,3-dione (0.95 g, 4.93 mmol) and magnesium bromide (8 mg, 0.045 mmol) were mixed in degassed DMA and stirred under an atmosphere of nitrogen at 90° C. for 90 min. 1M NaOH and EtOAc were added. The phases were separated and the organic solvents were evaporated. The residue was purified by flash chromatography with heptane/EtAc 20:1 to provide 1-(4-methoxyphenyl)-3-(methylthio)-1H-indole in 80% yield. ES/MS m/z: 270.11 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653072B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-a15b7cb847614fe0bf15da0edb31229b |
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| Quellennotiz | uspto-grants-2014_02 |
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