HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228523Generated: October 25, 2026
3,4-Dimethylphenol → 6,7-Dimethoxy-4-(3,4-dimethylphenoxy)quinoline
https://huagongshe.com/reaction/228523
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dimethylphenol | HCID 7249 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 6,7-Dimethoxy-4-(3,4-dimethylphenoxy)quinoline | HCID 23078387 | 58% |
Reaction Steps
4-Chloro-6,7-dimethoxyquinoline (200 mg) and 3,4-dimethylphenol (274 mg) were suspended in diethylene glycol dimethyl ether (0.1 ml), and the suspension was stirred at 180° C. for 1.5 hr. The reaction solution was cooled to room temperature, an aqueous sodium hydroxide solution was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was then washed with saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography on silica gel using acetone-chloroform to give 6,7-dimethoxy-4-(3,4-dimethylphenoxy)quinoline (160 mg, yield 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-3d14fea65c3846f2920e7e82745b8e7b |
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| Source note | uspto-grants-2009_07 |
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