HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213787Generated: October 25, 2026
Phosphorus oxychloride → 4-Chloro-7-methoxybenzo[g]quinoline-3-carbonitrile
https://huagongshe.com/reaction/2213787
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile | HCID 9813663 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-7-methoxybenzo[g]quinoline-3-carbonitrile | HCID 9835140 | 64.7% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105531B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-d5a4a73987734a63ab7d7d8587e7e1f4 |
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| Source note | uspto-grants-2006_09 |
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