HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 989342Erstellt: 23. Oktober 2026
Phosphorus oxychloride → 4-Chloro-7-methoxybenzo[g]quinoline-3-carbonitrile
https://huagongshe.com/de/reaction/989342
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | 7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile | HCID 9813663 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Chloro-7-methoxybenzo[g]quinoline-3-carbonitrile | HCID 9835140 | 64,7% |
Reaktionsschritte
A reaction mixture of 767.7 mg (3.1 mmol) of 7-methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile in 12 mL of phosphorus oxychloride and 5 drops of N,N-dimethylformamide (DMF) is refluxed for 2 hours. After cooling, the mixture is concentrated to dryness in vacuo to give a dark residue. The residue is partitioned between methylene chloride and ice-cooled saturated aqueous sodium carbonate solution. The organic layer is washed with ice-cooled brine and dried over sodium sulfate. The crude product is passed through a short column of silica gel, and further eluted with additional methylene chloride, followed by 95:5 methylene chloride/ethyl acetate. Removal of the solvent in vacuo yields 532.0 mg (64.7%) of 4-chloro-7-methoxybenzo[g]quinoline-3-carbonitrile as a bright yellow solid, mp 242-243° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06638929B2 |
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| Quelldatensatz | uspto-grants-2003_10 |
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| ORD ID | ord-6b6974e825fe4a5bb3fe38b39da320c7 |
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| Quellennotiz | uspto-grants-2003_10 |
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