Reacción #1144443

Ecuación de reacción

4-Pentylphenylacetylene

4-acetoxyphenyl iodide

toluene

→

4-(4′-Pentylphenyl)ethynyl phenol

Disolventes

diisopropylamine

Condiciones de reacción

Tratamiento posterior

1. 1
   Otroevaporated to dryness on a rotary evaporator
2. 2
   workup.DISSOLUTIONThe residue was redissolved in aqueous potassium hydroxide ethanolic solution
3. 3
   workup.STIRRINGstirred at 70° C. overnight
4. 4
   OtroThe mixture was evaporated to dryness
5. 5
   Otropartitioned between ethyl acetate and water
6. 6
   Otrothe organic phase was removed
7. 7
   Otrodried
8. 8
   Otroevaporated
9. 9
   OtroThe residue was purified by flash column chromatography
10. 10
    workup.WAITA pink coloured solid was left
11. 11
    Otroafter evaporation of the appropriate fractions
12. 12
    Otro1H-NMR and IR spectroscopy gave the expected signals

Procedimiento

4-Pentylphenylacetylene (10.5 g, 61.4 mmol), 4-acetoxyphenyl iodide (16.1 g, 61.4 mmol), a catalytic amount of Pd(PPh3)2Cl2 and a catalytic amount of copper iodide were stirred in diisopropylamine (100 ml) at 70° C. After 5 minutes, a precipitate was seen and the mixture became unstirrable, toluene (100 ml) was added. The mixture was stirred at room temperature for 24 hours and then evaporated to dryness on a rotary evaporator. The residue was redissolved in aqueous potassium hydroxide ethanolic solution and stirred at 70° C. overnight. The mixture was evaporated to dryness, then partitioned between ethyl acetate and water, the organic phase was removed, dried and evaporated. The residue was purified by flash column chromatography using DCM as eluant. A pink coloured solid was left after evaporation of the appropriate fractions. Yield=10.4 g, 64%. 1H-NMR and IR spectroscopy gave the expected signals.

Fuente