HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228528Generated: October 27, 2026
Water → 4-[(6-Bromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline
https://huagongshe.com/reaction/228528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-[(1,6-Dibromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline | HCID 68829718 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[(6-Bromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline | HCID 57756326 | 51.4% |
Reaction Steps
4-[(1,6-Dibromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline (65 mg) was dissolved in tetrahydrofuran (3 ml) to prepare a solution which was then cooled to −78° C. A 1.59 M n-butyllithium/hexane solution (0.4 ml) was added thereto, and the mixture was stirred at −78° C. for 20 min. Acetyl chloride (0.2 ml) was added to the reaction solution, and the mixture was stirred at room temperature overnight. Further, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using acetone-chloroform to give the title compound (28 mg, yield 51%).
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-2543c3d4a98242d88cc0c7131bc94f2e |
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| Source note | uspto-grants-2009_07 |
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