HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454135Generated: October 31, 2026
Sodium Hydroxide → 3-Fluoro-7-methoxy-2-methylquinoline
https://huagongshe.com/reaction/454135
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloro-3-fluoro-7-methoxyquinoline | HCID 22030591 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Fluoro-7-methoxy-2-methylquinoline | HCID 22030792 | 91% |
Reaction Steps
2-Chloro-3-fluoro-7-methoxyquinoline (210 g, 1 mmol), (prepared as described for the starting material in Example 157), in anhydrous THF (1 ml) was added to a mixture of copper(I)bromide (570 mg, 4.0 mmol) and methylmagnesium bromide (3.0M solution in diethyl ether, 2.7 ml, 8 mmol) in anhydrous THF (20 ml) at −78° C. The mixture was stirred for 1 hour at −78° C., allowed to warm to ambient temperature and then stirred for a further 18 hours. Saturated aqueous ammonium chloride solution and 5N aqueous sodium hydroxide solution (pH 12) were added and the product extracted with ethyl acetate (3×). The organic solution was washed with water, brine, dried (MgSO4) and evaporated to dryness to yield 3-fluoro-7-methoxy-2-methylquinoline (0.17 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492560B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ed7068db105d4f9788a278b38ebf3778 |
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| Source note | uspto-grants-2013_07 |
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