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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 428537Erstellt: 23. Oktober 2026

6-Methoxyquinoline → 5-Bromo-6-methoxyquinoline

https://huagongshe.com/de/reaction/428537

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-MethoxyquinolineHCID 14860—
EduktBromineHCID 24408—
EduktSodium BisulfiteHCID 23665763—
LösungsmittelAcetic AcidHCID 176—
Produkt5-Bromo-6-methoxyquinolineHCID 1841412858,7%

Reaktionsschritte

To a solution of 6-methoxyquinoline (5 g, 31.4 mmol) in acetic acid (50 mL) was slowly added Br2 neat (1.62 mL, 31.4 mmol). The reaction mixture was stirred at ambient temperature for 1 hour and then poured onto ice. Saturated aqueous sodium bisulfite was added, and the resulting slurry was extracted into EtOAc (2×200 mL). The organic fractions were combined, dried over Na2SO4, concentrated, and purified by column chromatography (5% MeOH/CH2Cl2) affording 4.39 g of the title compound as the acetate salt. The free base was prepared by washing the salt with 1 N NaOH (50 mL) and H2O (100 mL) and extracting into CH2Cl2 (200 mL). The organic fractions were concentrated affording 3.89 g (52%) of the title compound as a pink solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06313126B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-04db3afc05d0439e8c9082b013422ddd
Quellennotizuspto-grants-2001_11