Reaktion #2340591

Reaktionsgleichung

bromopentafluorobenzene

n-butyllithium

hexane

2-ethylpyrazolo[1,5-a]pyridine

→

title compound

Ausbeute 89.6%

7-Bromo-2-ethylpyrazolo[1,5-a]pyridine

Ausbeute 89.6%

Lösungsmittel

water

tetrahydrofuran

water

Ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe reaction mixture was stirred for 2 hours at below −70° C.
2. 2
   Extraktionextraction
3. 3
   ExtraktionThe organic extract
4. 4
   Waschenwas washed twice with 5% brine (50 mL)
5. 5
   Trocknendried over anhydrous magnesium sulfate
6. 6
   Sonstigethe solvent was evaporated under reduced pressure

Vorschrift

A solution of 2-ethylpyrazolo[1,5-a]pyridine (5.0 g, 34.2 mmol) in tetrahydrofuran (50 mL) was cooled to below −70° C. under a nitrogen stream, and then a solution of n-butyllithium in hexane (32.5 mL, 1.58M solution, 51.4 mmol) was added dropwise at below −60° C. After stirring for 1 hour, bromopentafluorobenzene (9.3 g, 37.7 mmol) was added dropwise to the reaction mixture at below −60° C. The reaction mixture was stirred for 2 hours at below −70° C., and then water (50 mL) was added to the reaction mixture and the temperature was raised to room temperature. Ethyl acetate (50 mL) and water (50 mL) were added thereto, and extraction was performed with ethyl acetate. The organic extract was washed twice with 5% brine (50 mL) and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure to afford 6.9 g of the title compound.

Quelle