HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743291Generated: November 2, 2026
Acetate → Ethyl 4-chloro-8-nitroquinoline-3-carboxylate
https://huagongshe.com/reaction/1743291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetate | HCID 175 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Ethyl 8-nitro-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 734639 | — |
| Product | Ethyl 4-chloro-8-nitroquinoline-3-carboxylate | HCID 11196760 | 89% |
Reaction Steps
To a solution of 8-Nitro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (10 g, 38.14 mmol) in 100 ml of thionyl chloride in a 250 ml round bottom flask was added a catalytic amount of 200 ul of dimethyl acetamide. The mixture was heated and refluxed for 2 hrs with stirring. The reaction was monitered by TLC (n-hexanelethyl acetate=3/1). After completing and cooling to room temperature, thiony chloride was removed under vacuum and 100 ml of water was added. The residue was extracted three times with 100 ml of ethyl acetate each time and the organic layer was dried over magnesium sulfate and filtrated. The residue was purified by column chromatography (hexan/ethyl acetate=3/1) to give 8-nitro-4-chloro-quinoline-3-carboxylic acid ethyl ester (9.5 g, 33.85 mmol, 89%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07009053B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-22c9c34720a24c868ca68f2d379aa5e1 |
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| Source note | uspto-grants-2006_03 |
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