HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75384Erstellt: 24. Oktober 2026
Carbon Tetrachloride → 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one
https://huagongshe.com/de/reaction/75384
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Tetrachloride | HCID 5943 | — |
| Edukt | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Edukt | Benzoyl Peroxide | HCID 7187 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 3-ethyl-7-fluoroquinoxalin-2(1H)-one | HCID 67289205 | — |
| Produkt | 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one | HCID 86698519 | 133% |
Reaktionsschritte
3-Ethyl-7-fluoroquinoxalin-2(1H)-one (20.61 g, 107.2 mmol) and 1,3-dibromo-5,5-dimethylhydantoin (18.77 g, 64.34 mmol) suspended in carbon tetrachloride (1072 ml, 107.2 mmol). To the heterogeneous mixture was added benzoyl peroxide (3.463 g, 10.72 mmol) and the mixture was heated at reflux with stirring (oil bath temperature: 80° C.) for 20 h. After 20 h, the mixture was cooled to rt. After cooling, the mixture was poured into saturated aqueous sodium bicarbonate solution (1 L) with stirring. The precipitate was collected by filtration and washed with water (1 L) to give 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one (23.19 g, 79.8% yield) as a tan solid:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835432B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-92849659d0874c5281220a124d720487 |
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| Quellennotiz | uspto-grants-2014_09 |
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