Reaktion #742101

ord-078415d80342456ab2945148936f90e0

Reaktionsgleichung

O=Cc1ccoc1
3-furaldehyde
[Br][Mg][CH2]CCc1ccccc1
3-phenylpropyl magnesium bromide
II
iodine
BrCCCc1ccccc1
1-bromo-3-phenylpropane
[Mg]
magnesium
O=S(=O)(O)O
sulfuric acid
OC(CCCc1ccccc1)c1ccoc1
alcohol
OC(CCCc1ccccc1)c1ccoc1
3-(1-Hydroxy-4-phenylbutyl)furan

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat 0°
  2. 2
    workup.ADDITIONpoured
  3. 3
    SonstigeThe resulting mixture was partitioned between ethyl ether and 5% sodium bisulfite
  4. 4
    WaschenThe organic portion was washed with 5% sodium bicarbonate solution, water, saturated sodium chloride solution
  5. 5
    Trocknendried over magnesium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated
  8. 8
    Sonstigeto give an oil
  9. 9
    SonstigeThis material was further purified by flash chromatography (silica, 20% ethyl acetate/hexane)

Vorschrift

To a stirred solution of 3-phenylpropyl magnesium bromide (4.5 ml of a 2.73M solution in ethyl ether, 12.3 mmol, generated from 1-bromo-3-phenylpropane and magnesium and initiated with iodine) at 0° under argon, was added dropwise 3-furaldehyde (1.08 g., 11.2 mmol) in 5 ml ethyl ether. This solution was allowed to warm to room temperature, stirred for 20 minutes, and then poured over crushed ice containing several drops of concentrated sulfuric acid. The resulting mixture was partitioned between ethyl ether and 5% sodium bisulfite. The organic portion was washed with 5% sodium bicarbonate solution, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give an oil. This material was further purified by flash chromatography (silica, 20% ethyl acetate/hexane) to give the desired alcohol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05134128uspto-grants-1992_07