HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7135Generated: October 26, 2026
3-Bromoquinoline → 3-Methoxyquinoline
https://huagongshe.com/reaction/7135
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromoquinoline | HCID 21413 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxyquinoline | HCID 575807 | 6.2% |
Reaction Steps
A solution of 3-bromoquinoline (22.54 g, 108 mmol) in anhydrous DMF (110 mL) was treated with sodium methoxide (11.70 g, 217 mmol) and stirred at 80° C. for 16 hours. The reaction mixture was then concentrated and the residue taken up in ethyl acetate (300 mL) and water (60 mL). The organic phase was separated, washed with brine (2×60 mL), dried (MgSO4), filtered, concentrated and purified by column chromatography on silica gel (ethyl acetate/hexane; 1:3) to give 3-methoxyquinoline (1.06 g, 6%). 1H NMR (CDCl3) δ 3.95 (s, 3H), 7.38 (d, 1H, J=1.5 Hz), 7.54 (m, 2H), 7.72 (d, 1H, J=7.5 Hz), 8.04 (d, 1H, J=7.5 Hz), 8.67 (d, 1H, J=1.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084155B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-5203239c158e446e9e84abab6abb16bf |
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| Source note | uspto-grants-2006_08 |
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