Réaction #531837

Équation de réaction

5-Bromo-2-chloropyridine

n-Butyllithium

formylpiperidine

→

2-chloro-5-formylpyridine

Rendement 63.5%

Solvants

diethyl ether

Diethyl ether

Conditions de réaction

Traitement

1. 1
   TempératureAfter the reaction vessel had been cooled to −70° C.
2. 2
   workup.WAITthe stirring was continued for another 60 minutes while the mixture
3. 3
   Autreto return to room temperature
4. 4
   AutreThe resulting reaction mixture
5. 5
   workup.ADDITIONmixed with it
6. 6
   Autreto separate organic
7. 7
   Extractionaqueous phases, and extraction
8. 8
   LavageThe combined organic phase was washed with water
9. 9
   Séchagedried over anhydrous magnesium sulfate
10. 10
    ConcentrationThe resulting solution was concentrated under reduced pressure
11. 11
    Autrethe residue was purified with a fractional operation by means of column chromatography (silica gel; toluene)
12. 12
    AutreThe product was further purified by recrystallization from heptane
13. 13
    workup.DISTILLATIONThe solvent was distilled off
14. 14
    Autrethe product was dried

Mode opératoire

5-Bromo-2-chloropyridine (T-9) (15.0 g) and diethyl ether (450 ml) were put in a reaction vessel and cooled to −50° C. under an atmosphere of nitrogen. n-Butyllithium (1.57 M in n-hexane; 54.6 ml) was added dropwise in the temperature range of −50° C. to −45° C., and the stirring was continued for another 90 minutes. After the reaction vessel had been cooled to −70° C., formylpiperidine (9.70 g) was added dropwise in the temperature range of −70° C. to −65° C., and the stirring was continued for another 60 minutes while the mixture was allowed to return to room temperature. The resulting reaction mixture was poured into ice-water (500 ml) and mixed with it. Diethyl ether (200 ml) was added to the solution to separate organic and aqueous phases, and extraction was carried out. The combined organic phase was washed with water and dried over anhydrous magnesium sulfate. The resulting solution was concentrated under reduced pressure and the residue was purified with a fractional operation by means of column chromatography (silica gel; toluene). The product was further purified by recrystallization from heptane. The solvent was distilled off and the product was dried, giving 2-chloro-5-formylpyridine (T-10) (7.01 g). The yield based on the compound (T-9) was 68%.

Source