Reaktion #9282

ord-c955a68fd91c4d9193e9298121138839

Reaktionsgleichung

COc1cccnc1Br
2-bromo-3-methoxypyridine
C#CCC
1-butyne
CCNCC
diethylamine
CCC#Cc1cc(OC)ccn1
2-(1-butynyl)-4-methoxypyridine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas bubbled through at room temperature
  2. 2
    SonstigeUpon completion of the reaction
  3. 3
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  4. 4
    workup.ADDITIONWater was added to the obtained residue, extraction
  5. 5
    Waschenthe extract was washed with brine
  6. 6
    Trocknendried over magnesium sulfate
  7. 7
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure

Vorschrift

After adding dichlorobis(triphenylphosphine)palladium (II) (671 mg) and copper iodide (91 mg) to a solution of 2-bromo-3-methoxypyridine (18.0 g) in diethylamine (250 mL), 1-butyne (15.5 g) was bubbled through at room temperature, and the mixture was stirred for 20 hours. Upon completion of the reaction, the solvent was distilled off under reduced pressure. Water was added to the obtained residue, extraction was performed with ethyl acetate, the extract was washed with brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was subjected to silica gel column chromatography (500 g), and 2-(1-butynyl)-4-methoxypyridine (10.0 g) was obtained from the n-hexane:ethyl acetate (2:1) fraction as a brown oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091215B2uspto-grants-2006_08