HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987572Generated: October 30, 2026
Hydrogen Bromide → 8-bromo-6-methoxyquinoline
https://huagongshe.com/reaction/987572
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Methoxy-8-quinolinamine | HCID 7023 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Product | 8-bromo-6-methoxyquinoline | HCID 279599 | 61% |
Reaction Steps
To 5.05 g (29.0 mmol) 6-methoxy-quinolin-8-yl-amine in 25 mL of 48% HBr at 0° C. is added a solution of 2.60 g (37.7 mmol) and 20 mL H2O. After stirring at 0° C. for 15 min, the resulting mixture is added dropwise to a 75° C. solution of 5.0 g (34.8 mmol) CuBr and 60 mL of 48% HBr. After 5.5 h, the reaction mixture is neutralized with 150 mL of ice cold 5N NaOH, the resulting mixture is stirred with 300 mL EtOAc and filtered through a pad of celite. This mixture is extracted 2×100 mL EtOAc, and the combined organics are washed with 1×200 mL H2O, 1×200 mL brine, dried over Na2SO4, filtered, and the volatiles are evaporated. Flash chromatography on SiO2 gel, eluting with hexanes/EtOAc (4/1 to 1/1), gives 4.23 g (17.8 mmol, a 61% yield) of the title compound as a brown oil. MS (ES) m/z 239 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06632824B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-cb6e14c7a8914d30982d7723ab142908 |
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| Source note | uspto-grants-2003_10 |
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