Reaktion #732498

Reaktionsgleichung

1-chloro-6-bromo-2-naphthol

→

1-chloro-6-(1-pentynyl)-2-naphthol

Ausbeute 177.5%

Lösungsmittel

triethylamine

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe compound (S7-3) was synthesized
2. 2
   Sonstigedisclosed in Synthesis
3. 3
   workup.ADDITIONwas added
4. 4
   Temperaturby refluxing for 6 hours
5. 5
   TemperaturThe reaction mixture was cooled to room temperature
6. 6
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
7. 7
   workup.ADDITIONEthyl acetate was added to the resulting residue
8. 8
   Filtrationthe mixture was filtered with Celite
9. 9
   WaschenThe resulting solution was washed with 1N hydrochloric acid and water
10. 10
    Trocknendried over anhydrous magnesium sulfate
11. 11
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
12. 12
    Sonstigethe resulting residue was purified by silica gel column chromatography with a mixed solvent of heptane and ethyl acetate (3/1) as a developing solvent
13. 13
    Sonstigedried under reduced pressure

Vorschrift

The compound (S7-3) was synthesized according to the method disclosed in Synthesis, No. 9, 1439 (2004). 38.3 g of 1-chloro-6-bromo-2-naphthol (S1-2), 5.2 g of PdCl2(PPh3)2, 0.71 g of copper iodide and 400 mL of triethylamine were added to a reactor under a nitrogen atmosphere and stirred at room temperature, to which 35.8 g of 1-heptine (S7-2) was added, followed by refluxing for 6 hours. The reaction mixture was cooled to room temperature, and the solvent was distilled off under reduced pressure. Ethyl acetate was added to the resulting residue, and the mixture was filtered with Celite. The resulting solution was washed with 1N hydrochloric acid and water, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography with a mixed solvent of heptane and ethyl acetate (3/1) as a developing solvent and dried under reduced pressure to provide 32.3 g of 1-chloro-6-(1-pentynyl)-2-naphthol (S7-3).

Quelle