HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325626Generated: October 30, 2026
Dimethyl Sulfate → 3-Hydroxymethyl-1-methyl-7-trifluoromethyl-4-quinolone
https://huagongshe.com/reaction/325626
Participants
| Role | Name | HCID | Charge |
|---|
| 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 |
|---|
| Patent number | US04442109 |
|---|
| Source dataset | uspto-grants-1984_04 |
|---|
| ORD ID | ord-e4e1e9f7cd034cd0a060df575ded78f8 |
|---|
| Source note | uspto-grants-1984_04 |
|---|