HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1887796Erstellt: 25. Oktober 2026
Azobisisobutyronitrile → 3-bromomethyl-7-chloro-1-phenyl-1H-quinolin-4-one
https://huagongshe.com/reaction/1887796
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 7-chloro-3-methyl-1-phenyl-1H-quinolin-4-one | HCID 71208522 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | 3-bromomethyl-7-chloro-1-phenyl-1H-quinolin-4-one | HCID 86675764 | — |
Reaktionsschritte
In a 50 mL round-bottomed flask, 7-chloro-3-methyl-1-phenyl-1H-quinolin-4-one (0.142 g, 0.526 mmol), NBS (103 mg, 0.579 mol) and AIBN (13.0 mg, 0.079 mmol) were combined with carbon tetrachloride (3.5 mL) to give a colorless solution. The reaction mixture was heated at 115° C. for 1 h. The reaction mixture was cooled to room temp and then cooled to 0° C. The mixture was filtered to remove succinimide and the filtrate was concentrated. The crude product was used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08501732B2 |
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| Quelldatensatz | uspto-grants-2013_08 |
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| ORD ID | ord-92c9e29e40264b41b7ed6f9bc1c9ee64 |
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| Quellennotiz | uspto-grants-2013_08 |
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