Réaction #1340986

Équation de réaction

ammonium chloride

5-bromo-2-hydroxy-4-methylpyridine

sodium hydride

3-hydroxy-3-methylbutyl 4-methylbenzene sulfonate

→

compound

Rendement 63.1%

4-(5-bromo-4-methylpyridin-2-yloxy)-2-methylbutan-2-ol

Rendement 63.1%

Solvants

N,N-dimethylformamide

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONwas added
2. 2
   Températurecooling
3. 3
   Autrethe resultant reaction mixture
4. 4
   Autrethe resultant reaction mixture
5. 5
   workup.STIRRINGwas stirred at 60° C. for 4 hours
6. 6
   Autrethe resultant reaction mixture
7. 7
   Extractionwas extracted with ethyl acetate
8. 8
   LavageThe organic phase was washed with a saturated saline
9. 9
   Séchagewas dried over anhydrous sodium sulfate
10. 10
    workup.DISTILLATIONFrom the organic phase, the solvent was distilled off under reduced pressure
11. 11
    Autrethe resultant residue was purified by silica gel column chromatography (eluate; n-hexane:ethyl acetate=50:50 to 33:67)

Mode opératoire

To a suspension of sodium hydride (to which about 40% of a mineral oil was added, 0.23 g) in N,N-dimethylformamide (10 mL), 5-bromo-2-hydroxy-4-methylpyridine (1.00 g) was added under ice-cooling and the resultant reaction mixture was stirred for 30 minutes. To the reaction mixture, 3-hydroxy-3-methylbutyl 4-methylbenzene sulfonate (1.51 g) was added and the resultant reaction mixture was stirred at 60° C. for 4 hours. To the reaction mixture, a saturated ammonium chloride aqueous solution was added and the resultant reaction mixture was extracted with ethyl acetate. The organic phase was washed with a saturated saline and was dried over anhydrous sodium sulfate. From the organic phase, the solvent was distilled off under reduced pressure and the resultant residue was purified by silica gel column chromatography (eluate; n-hexane:ethyl acetate=50:50 to 33:67) to obtain the subject compound (0.92 g) as a pale yellow oil.

Source