HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852985Generated: October 29, 2026
6-Bromo-4-chloroquinoline → 6-Bromo-4-methoxyquinoline
https://huagongshe.com/reaction/852985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Bromo-4-chloroquinoline | HCID 5139537 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-4-methoxyquinoline | HCID 45790929 | 90.8% |
Reaction Steps
To a solution of 6-bromo-4-chloro-quinoline (12.12 g, 50 mmol) in methanol (200 mL) was added sodium methoxide (13.50 g, 250 mmol) at room temperature. Then, the reaction mixture was heated to 120° C. for 15 h in a sealed reaction flask. After cooling to room temperature, the methanol was removed under the vacuum and the residue was diluted with water. Then, the solids were collected by filtration and washed with water. After drying in air, 10.8 g (90.8% yield) of 6-bromo-4-methoxy-quinoline was isolated as a white solid which can be crystallized from acetonitrile: EI-HRMS m/e calcd for C10H8BrNO (M+) 236.9789, found 236.9784.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253285B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-61b3efb569674f40803d27245218fd78 |
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| Source note | uspto-grants-2007_08 |
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