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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987572Generated: October 30, 2026

Hydrogen Bromide → 8-bromo-6-methoxyquinoline

https://huagongshe.com/reaction/987572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantWaterHCID 962—
Reactant6-Methoxy-8-quinolinamineHCID 7023—
ReactantEthyl AcetateHCID 8857—
Product8-bromo-6-methoxyquinolineHCID 27959961%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632824B2
Source datasetuspto-grants-2003_10
ORD IDord-cb6e14c7a8914d30982d7723ab142908
Source noteuspto-grants-2003_10