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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-4-chloroquinolineHCID 5139537—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product6-Bromo-4-methoxyquinolineHCID 4579092990.8%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253285B2
Source datasetuspto-grants-2007_08
ORD IDord-61b3efb569674f40803d27245218fd78
Source noteuspto-grants-2007_08