HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24136Erstellt: 24. Oktober 2026
Water → 6-Bromo-1,4,4-trimethyl-3,4-dihydroquinolin-2(1H)-one
https://huagongshe.com/de/reaction/24136
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Edukt | N-(4-Bromophenyl)-N-methyl-3-methyl-2-butenamide | HCID 22568913 | — |
| Lösungsmittel | Methylenechloride Hexane | HCID 21226440 | — |
| Produkt | 6-Bromo-1,4,4-trimethyl-3,4-dihydroquinolin-2(1H)-one | HCID 22569003 | 26,4% |
Reaktionsschritte
N-(4-bromophenyl)-N-methyl-3-methyl-2-butenamide (Intermediate 54, 6.42 g, 24 mmol) was heated to 130° C. and aluminum chloride (5 g, 37.4 mmol) was added in portions over 0.5 h. The reaction mixture was stirred for 1 hour at the same temperature and then cooled to room temperature. Ice was added cautiously to the solid, followed by ˜200 mL of iced water. The reaction mixture was then extracted with ether (×2) and dichloromethane (×1) and the combined organic phase was dried over anhydrous magnesium sulfate and evaporated in vacuo to yield a brown solid. The solid was treated with hexane-dichloromethane and filtered to afford 1.7 g of product. The mother liquor was evaporated and purified by flash column chromatography on silica gel (230-400 mesh) to afford 2.9 g of the title compound as a solid (total 72%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06855512B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-b85b6f9e5d254a01ae011c966d72a4e5 |
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| Quellennotiz | uspto-grants-2005_02 |
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