Reacción #1820952

Ecuación de reacción

ethyl 10-bromoundecanoate

3-iodophenol

potassium carbonate

EtOAc

→

ethyl 10-(3-iodophenoxy)-undecanoate

Rendimiento 33.3%

Disolventes

DMF

DMF

—

hexanes

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe reaction was immersed in an oil bath
2. 2
   Temperaturathe oil bath temperature was increased to 85° C
3. 3
   workup.STIRRINGAfter stirring for an additional 4 hrs at 85° C.
4. 4
   Temperaturato cool
5. 5
   Filtraciónfiltered through a pad of celite
6. 6
   Otroevaporated in vacuo
7. 7
   LavadoThe organic phase was washed with water (100 ml), 1M aqueous sodium hydroxide (100 ml), water (2×100 ml) and brine (100 ml)
8. 8
   Secadodried (Na2SO4)
9. 9
   Filtraciónfiltered
10. 10
    Otroevaporated in vacuo
11. 11
    Otroto provide crude ethyl 10-(3-iodophenoxy)undecanoate which

Procedimiento

To a stirred solution of ethyl 10-bromoundecanoate (9.7 g, 33.0 mmol) in dry DMF (66 ml) was added 3-iodophenol (7.99 g, 36.3 mmol) and potassium carbonate (5.02 g, 37.6 mmol). The reaction was immersed in an oil bath which was warmed to 75° C. over 0.5 hr. After stirring for 14 hrs under an N2 atmosphere, the oil bath temperature was increased to 85° C. After stirring for an additional 4 hrs at 85° C., the reaction was allowed to cool, diluted with DMF (200 ml), filtered through a pad of celite and evaporated in vacuo. The resulting residue was taken up in ether (500 ml). The organic phase was washed with water (100 ml), 1M aqueous sodium hydroxide (100 ml), water (2×100 ml) and brine (100 ml), dried (Na2SO4), filtered and evaporated in vacuo to provide crude ethyl 10-(3-iodophenoxy)undecanoate which was contaminated with olefinic esters. Flash column chromatography (silica, 1-2%; EtOAc in hexanes) provide ethyl 10-(3-iodophenoxy)-undecanoate as a clear oil (4.75 g, 33.3%).

Fuente