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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 455696Erstellt: 24. Oktober 2026

N-bromobutanimide → 3-Bromo-2-fluoro-6-(neopentyloxy)pyridine

https://huagongshe.com/de/reaction/455696

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt2-Fluoro-6-(neopentyloxy)pyridineHCID 57475658—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-Bromo-2-fluoro-6-(neopentyloxy)pyridineHCID 5747565951,8%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

N-bromosuccinimide (8.29 g, 46.6 mmol) was added to a solution of 2-fluoro-6-(neopentyloxy)pyridine (7.11 g, 38.8 mmol) in acetonitrile (80 mL) at rt. The reaction mixture was heated to 70° C. overnight. The reaction mixture was cooled to rt and the solvent was removed under reduced pressure. The residue was dissolved in DCM and washed with water. The organic layer was separated, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (100% hexanes) to obtain 3-bromo-2-fluoro-6-(neopentyloxy)pyridine (5.27 g, 20.11 mmol) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08497264B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-4d5c88843d5f4cb193de66352cd81375
Quellennotizuspto-grants-2013_07