Reaktion #44326

Reaktionsgleichung

1-bromo-2,4-difluorobenzene

2-bromopyridine

hexane

n-butyllithium

→

2-(2,4-difluorophenyl)pyridine

Ausbeute 63.0%

Lösungsmittel

tetrahydrofuran

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeover 30 minutes
2. 2
   Sonstigewas slowly elevated to 0° C.
3. 3
   Temperaturunder reflux
4. 4
   workup.ADDITION200 ml of saturated saline was added to the reaction mixture
5. 5
   Extraktionfollowed by extraction of the reaction mixture with diethyl ether
6. 6
   SonstigeAfter drying
7. 7
   Einengenthe extract, concentration and purification by column chromatography (silica gel; chloroform/hexane (1/1: volume ratio))

Vorschrift

That is, under argon stream, 8.69 g (55.0 mmol) of 2-bromopyridine was dissolved in 200 ml of dry tetrahydrofuran and cooled to −78° C. To this was dripped 38.7 ml (61.9 mmol) of a 1.6 M hexane solution of n-butyllithium over 30 minutes. After completion of the dripping, further a solution of 7.5 g (55.0 mmol) of zinc chloride in 50 ml of dry tetrahydrofuran was dripped over 30 minutes. After completion of the dripping, the temperature of the mixture was slowly elevated to 0° C. and 9.65 g (55.0 mmol) of 1-bromo-2,4-difluorobenzene and 2.31 g (2.0 mmol) of tetrakis(triphenylphosphine)palladium (0) were added thereto. The mixture was stirred for 6 hours under reflux and then 200 ml of saturated saline was added to the reaction mixture, followed by extraction of the reaction mixture with diethyl ether. After drying the extract, concentration and purification by column chromatography (silica gel; chloroform/hexane (1/1: volume ratio)) afforded 6.00 g (31.4 mmol) of 2-(2,4-difluorophenyl)pyridine as colorless transparent oil. Yield: 63%. Identification was performed by elementary analysis of 1H-NMR and elementary analysis of C, H and N.

Quelle