HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613941Generated: November 2, 2026
Hydrochloric Acid → 2-(trans-1-Hydroxy-2-nonenyl)-3-methyl-6-fluoro-4-quinolone
https://huagongshe.com/reaction/1613941
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(trans-1-Hydroxy-2-nonenyl)-3-methyl-4-acetoxy-6-fluoroquinoline | HCID 15007063 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(trans-1-Hydroxy-2-nonenyl)-3-methyl-6-fluoro-4-quinolone | HCID 86746631 | 72.4% |
Reaction Steps
A solution of 715 mg (5.18 mmols) of potassium carbonate in 3 ml of water was added to a solution of 1.86 g (5.18 mmols) of 2-(trans-1-hydroxy-2-nonenyl)-3-methyl-4-acetoxy-6-fluoroquinoline, 50 ml of methanol and 2 ml of water and stirred at room temperature for 10 minutes. After neutralization by addition of 1N hydrochloric acid, the solvent was distilled off under reduced pressure and 30 ml of chloroform was added to the resultant residue, followed by washing with water and drying with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the resultant residue was purified by silica gel column chromatography (solvent: chloroform : methanol=40:1) to obtain 1.19 g (yield 72 %) of 2-(trans-1-hydroxy-2-nonenyl)-3-methyl-6-fluoro-4-quinolone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05194617 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-aece128e6fbb414aa508fe8a0386b301 |
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| Source note | uspto-grants-1993_03 |
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