HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25516Erstellt: 24. Oktober 2026
Methyl iodide → [5-(1H-Indol-2-yl)-2-methoxy-phenyl]-methyl-amine
https://huagongshe.com/de/reaction/25516
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 5-(1H-indol-2-yl)-2-methoxy-phenylamine | HCID 9900204 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | [5-(1H-Indol-2-yl)-2-methoxy-phenyl]-methyl-amine | HCID 9921288 | 27% |
Reaktionsschritte
In acetone (50 mL) was placed 5-(1H-indol-2-yl)-2-methoxy-phenylamine (2.38 g, 10 mmol). To this was added potassium carbonate (5.53 g, 40 mmol), and to the vigorously stirred mixture was added methyl iodide (1.55 g, 11 mmol). The mixture warmed to 40° C. and stirred for 48 hours. The mixture cooled to room temperature and was filtered free of inorganics. The resulting solution was evaporated in vacuo to give a solid which was partitioned between ethyl acetate (50 mL) and water (50 mL). The organic phase was separated, dried over magnesium sulfate, and evaporated in vacuo to give a tan solid. This solid was purified by flash chromatography over silica gel (5% ethyl acetate/methylene chloride). Evaporation of the appropriate fractions gave 0.68 g of pure compound. MS: M+1=253.1. 1H NMR (DMSO-d6) δ 2.79 (d, J=5.3 Hz, 3H), 3.80 (s, 3H), 5.08-5.12 (m, 1H), 6.69 (s, 1H), 6.83-7.05 (m, 5H), 7.33 (d, J=7.9 Hz, 1H), 7.44 (d, J=8.0 Hz, 1H), 11.28 (s, 1H) ppm.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06858739B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-5c508525b84f40e6abab25c56de6090c |
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| Quellennotiz | uspto-grants-2005_02 |
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