Reaktion #7558
ord-955645a8fc6a4fd1b0144ff9ec621f18
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONwas added to the solution
- 2Temperaturunder ice-cooling
- 3Sonstigethe organic layer was separated
- 4WaschenThe organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution
- 5Trocknena saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
- 6workup.DISTILLATIONdistilled under reduced pressure
- 7Sonstigeto remove the solvent
- 8workup.ADDITIONDiethyl ether was added to the residue
- 9Filtrationthe insoluble materials were filtered off
- 10workup.DISTILLATIONafter which the solvent was distilled off under reduced pressure
- 11SonstigeThe residue was purified by a column chromatography (eluent; hexane:ethyl acetate=20:1 to 10:1)
Vorschrift
In 40 mL of methylene chloride was dissolved 2.00 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]-1-propanol, and 5.55 g of triphenylphosphine was added to the solution, after which a solution of 8.42 g of carbon tetrabromide in 10 mL of methylene chloride was added dropwise thereto under ice-cooling and the resulting mixture was stirred at room temperature for 20 minutes. To the reaction mixture was added 20 mL of water, and the organic layer was separated. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. Diethyl ether was added to the residue and the insoluble materials were filtered off, after which the solvent was distilled off under reduced pressure. The residue was purified by a column chromatography (eluent; hexane:ethyl acetate=20:1 to 10:1) to obtain 1.93 g of 5-[2-(3-bromopropoxy)ethyl]-1-benzothiophene as a colorless oil.