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HRID 2212583Erstellt: 25. Oktober 2026
Water → 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one
https://huagongshe.com/reaction/2212583
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Iodoethane | HCID 6340 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 7-Bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one | HCID 21966423 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one | HCID 21966429 | 104,5% |
Reaktionsschritte
A mixture of powdered potassium hydroxide (3.35 g, 59.67 mmol) in DMSO (40 mL) was stirred at 0° C. for 10 min. 7-bromo-4,4,6-trimethyl-3,4- dihydro-1H-quinoline-2-one (Example 1e) (8.0 g, 29.83 mmol) was added cautiously, followed immediately by the addition of ethyl iodide (12 mL, 149.17 mmol). The reaction mixture was kept at 0° C. for 30 min then slowly warmed up to room temperature and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with dichloromethane washed with water and brine, dried (MgSO4), filtered and evaporated to give 8.8 g of 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one and used without further purification in the Suzuki coupling (step a): 1H NMR (300 MHz; CDCl3): 1.24 (t, J=7.2 Hz, 1 H), 1.25 (s, 6 H), 2.37 (s, 3 H), 2.45 (s, 2 H), 3.98 (q, 2 H), 7.13 (s, 1 H), 7.18 (s, 1 H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07102000B2 |
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| Quelldatensatz | uspto-grants-2006_09 |
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| ORD ID | ord-65611467eb1f4fa994c040d3141ab846 |
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| Quellennotiz | uspto-grants-2006_09 |
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