HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852989Generated: October 29, 2026
Sodium ethoxide → 6-Bromo-4-ethoxyquinoline
https://huagongshe.com/reaction/852989
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 6-Bromo-4-chloroquinoline | HCID 5139537 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 6-Bromo-4-ethoxyquinoline | HCID 58615398 | 90.2% |
Reaction Steps
To a solution of 6-bromo-4-chloroquinoline (17 g, 70.10 mmol) in ethanol (400 mL) was added sodium ethoxide (23.85 g, 350.5 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 ethanol was removed under the vacuum and the residue was diluted with water. The aqueous suspension was neutralized with 3.0N hydrochloric acid until the precipitate formed and later it was diluted with saturated sodium bicarbonate solution. Then, the solids were collected by filtration and washed with water. After drying in air, 15.94 g (90.2% yield) of 6-bromo-4-ethoxy-quinoline was isolated as a white solid which can be crystallized from acetonitrile: EI-HRMS m/e calcd for C11H10BrNO (M+) 250.9946, found 250.9946.
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-5b83827849b44cdf8ee3784a67aae9a0 |
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| Source note | uspto-grants-2007_08 |
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