HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543674Generated: October 31, 2026
Dimethyl Sulfate → 3-Hydroxymethyl-1-methyl-7-trifluoromethyl-4-quinolone
https://huagongshe.com/reaction/543674
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178519811 | HCID 178519811 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Hydroxymethyl-1-methyl-7-trifluoromethyl-4-quinolone | HCID 12807882 | — |
Reaction Steps
Dimethyl sulphate (24.4 g.) was added over 5 minutes to a stirring solution of 4-hydroxy-3-hydroxymethyl-7-trifluoromethylquinoline (23.6 g.) and potassium hydroxide (16.3 g.) in a mixture of water (50 ml.) and tetrahydrofuran (50 ml.) at room temperature. After stirring for a further 3 hours at this temperature the solid product was collected. The filtrate was extracted with dichloromethane (3×200 ml.). The combined extracts were dried over anhydrous magnesium sulphate and evaporated to give a second crop of the solid. The combined solids were purified by high pressure liquid chromatography over silica gel, eluting with isopropanol: dichloromethane 10:90 at a flow rate of 200 ml. per minute. The same solvent was used for applying the product to silica gel. This procedure gave the novel 3-hydroxymethyl-1-methyl-7-trifluoromethyl-4-quinolone, m.p. 172°-175°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04447435 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-f57a1e8709694c2bb612d87c89df51e2 |
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| Source note | uspto-grants-1984_05 |
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