HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339002Generated: October 26, 2026
Potassium Carbonate → 8-Fluoro-7-(2-methoxyethoxy)-2-methylquinoline
https://huagongshe.com/reaction/339002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | 8-Fluoro-2-methylquinolin-7-ol | HCID 136338078 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 8-Fluoro-7-(2-methoxyethoxy)-2-methylquinoline | HCID 70983264 | 54.6% |
Reaction Steps
To a mixture of 8-fluoro-2-methylquinolin-7-ol (0.30 g, 1.69 mmol) and potassium carbonate (0.70 mg, 5.08 mmol) in acetone (7 mL) was added 1-bromo-2-methoxyethane (0.47 g, 3.39 mmol) and the mixture heated at 70° C. for 18 hours. Additional bromo-2-methoxyethane (0.150 mL) and potassium carbonate (0.35 g) were added and heating was continued for 16 hours. The mixture was partitioned between water and ethyl acetate and the layers were separated. The organic layer was dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by column chromatography (Biotage, 25M; 25% ethyl acetate:hexanes) to afford 8-fluoro-7-(2-methoxyethoxy)-2-methylquinoline (0.217 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889704B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-be6da6fc5ee34d0b8a65eb10491e6dd4 |
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| Source note | uspto-grants-2014_11 |
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