3-Bromo-2-fluoropyridine → 3-Bromo-2-(tert-butoxy)pyridine

HRID 403669

Reaktionsgleichung

Reaktionsgleichung von HRID 403669
[Br:1][C:2]1[C:3](F)=[N:4][CH:5]=[CH:6][CH:7]=1.[CH3:9][C:10]([CH3:13])([O-:12])[CH3:11].[K+]>O1CCCC1>[Br:1][C:2]1[C:3]([O:12][C:10]([CH3:13])([CH3:11])[CH3:9])=[N:4][CH:5]=[CH:6][CH:7]=1

Komponenten

4

Versuchsvorschrift

To a solution of 3-bromo-2-fluoropyridine (500 mg, 2.84 mmol) in anhydrous tetrahydrofuran (10 mL) under nitrogen was added potassium tert-butoxide (540 mg, 4.8 mmol) in portions over 30 minutes at 25° C., and stirring was continued for 4 hours at 25° C. The mixture was concentrated in vacuo and purified by silica gel flash chromatography eluting with dichloromethane/hexanes (50% to 100%) to give the title compound.

Aufarbeitung

  1. concentrationThe mixture was concentrated in vacuo
  2. custompurified by silica gel flash chromatography
  3. washeluting with dichloromethane/hexanes (50% to 100%)

Quellen und Nachweise

ORD-Eintrag
ord-0763c82d1c184bd2a568fb0059e68e7a
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08748443B2

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