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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2782Erstellt: 24. Oktober 2026

4-Bromoaniline → 6-Bromoquinolin-2(1H)-one

https://huagongshe.com/de/reaction/2782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromoanilineHCID 7807—
Edukt3-Phenylprop-2-enoyl chlorideHCID 66023—
Produkt6-Bromoquinolin-2(1H)-oneHCID 12378943—
Produkt6-Bromo-2-chloroquinolineHCID 12894086—

Reaktionsschritte

The title compound is prepared from 4-bromoaniline and cinnamoyl chloride according to the procedure described in J. Chem. Soc., Perkin Trans. I, 1972, 1648. The crude 6-bromo-1H-quinolin-2-one intermediate obtained is triturated in Et2O/hexanes and filtered to give a beige solid which is used directly in the chlorination step. The crude product is recrystallized in MeOH to afford the title compound as a beige solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731315
Quelldatensatzuspto-grants-1998_03
ORD IDord-d45dd22efe384d6e8d41b31969ccab08
Quellennotizuspto-grants-1998_03