HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 703235Erstellt: 24. Oktober 2026
Sodium Hydroxide → 1-(5-Methoxy-2-methyl-1H-indol-3-yl)ethanone
https://huagongshe.com/de/reaction/703235
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | Dimethylacetamide | HCID 31374 | — |
| Edukt | 5-Methoxy-2-methylindole | HCID 70642 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(5-Methoxy-2-methyl-1H-indol-3-yl)ethanone | HCID 604823 | 67,2% |
Reaktionsschritte
Dimethylacetamide (17.5 ml, 188.4 mmol) is added dropwise with stirring to phosphorous oxychloride (12.9 ml, 138.2 mmol) at 0° C. Stirring is maintained for 45 minutes, at which time the bath is removed and 5-methoxy-2-methylindole (20.25 g, 125.6 mmol) in 15 ml of dimethylacetamide is added dropwise over a period of 75 minutes. The resulting mixture is warmed to 40°-45° C. for 4 hours. The reaction mixture is cooled to 0° C., and 100 g of ice water is added followed by dropwise addition of a solution of sodium hydroxide (50 g) in water (75 ml). The first 1/3 of this sodium hydroxide solution is added slowly and the remainder is added quickly. The exothermic reaction is quickly warmed to boiling for 15 minutes, cooled to room temperature and refrigerated overnight. The resulting crystals are collected by filtration and rinsed four times with water. Recrystallization from ethanol/water gives 17.2 g (67.2%) of pure 1-(5-methoxy-2-methyl-1H-indol-3-yl)ethanone; mp 229.0°-230.5° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04981865 |
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| Quelldatensatz | uspto-grants-1991_01 |
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| ORD ID | ord-aaba1a13538846a08358f100659875e4 |
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| Quellennotiz | uspto-grants-1991_01 |
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