Reaktion #7558

ord-955645a8fc6a4fd1b0144ff9ec621f18

Reaktionsgleichung

O
water
OCCCOCCc1ccc2sccc2c1
3-[2-(1-benzothiophen-5-yl)ethoxy]-1-propanol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
BrC(Br)(Br)Br
carbon tetrabromide
BrCCCOCCc1ccc2sccc2c1
5-[2-(3-bromopropoxy)ethyl]-1-benzothiophene
Ausbeute 76.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added to the solution
  2. 2
    Temperaturunder ice-cooling
  3. 3
    Sonstigethe organic layer was separated
  4. 4
    WaschenThe organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution
  5. 5
    Trocknena saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONdistilled under reduced pressure
  7. 7
    Sonstigeto remove the solvent
  8. 8
    workup.ADDITIONDiethyl ether was added to the residue
  9. 9
    Filtrationthe insoluble materials were filtered off
  10. 10
    workup.DISTILLATIONafter which the solvent was distilled off under reduced pressure
  11. 11
    SonstigeThe 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087594B2uspto-grants-2006_08