HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090048Generated: October 31, 2026
Sodium Methoxide → 5-Bromo-8-fluoro-2-methoxyquinoline
https://huagongshe.com/reaction/2090048
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 5-Bromo-2-chloro-8-fluoroquinoline | HCID 58349446 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-8-fluoro-2-methoxyquinoline | HCID 67304250 | — |
Reaction Steps
To a suspension of 5-bromo-2-chloro-8-fluoroquinoline (1.08 g, 4.2 mmol) in anhydrous methanol (10 mL) at 50° C. was added NaOMe (30% w/w, 0.9 g, 5.0 mmol). The resulting mixture was stirred at 50° C. for one hour, then allowed to cool to room temperature. The mixture was diluted with water, then extracted with EtOAc. The combined organics were washed with water then saturated Nael (aq), dried over MgSO4, filtered, then concentrated. The residue was purified by silica gel chromatography eluting with 0-5% EtOAc/hexanes to afford the title compound as a white solid: 1H NMR (500 MHz, CDCl3): δ 8.33 (dd, J=9.1, 1.6 Hz, 1H); 7.55 (dd, J=8.4, 4.4 Hz, 1H); 7.22 (dd, J=10.2, 8.4 Hz, 1H); 7.04 (d, J=9.2 Hz, 1H); 4.13 (s, 4H). LC4 2.37 min. (M+H) 256.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436015B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-cb6aa7a2549542e6b90d17010680ef19 |
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| Source note | uspto-grants-2013_05 |
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