Reaktion #74591

Reaktionsgleichung

tert-butyl(chloro)dimethylsilane

4-chloro-2-iodophenol

1H-imidazole

→

title compound

Ausbeute 95.0%

tert-Butyl(4-chloro-2-iodophenoxy)dimethylsilane

Ausbeute 95.0%

Lösungsmittel

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Einengenbefore concentrating in vacuo
2. 2
   workup.ADDITIONThe residue was diluted with ethyl acetate (20 ml) and water (20 ml)
3. 3
   Extraktionextracted with ethyl acetate
4. 4
   WaschenThe combined organic layers were washed with hydrochloric acid (2 M aqueous solution), saturated aqueous sodium chloride solution
5. 5
   Trocknendried over sodium sulfate
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated in vacuo
8. 8
   SonstigeThe residue was purified by column chromatography (40 g silica gel column)
9. 9
   Wascheneluting with ethyl acetate

Vorschrift

To a solution of 4-chloro-2-iodophenol (1.587 g, 6.238 mmol) in dichloromethane (10 ml) was added 1H-imidazole (1.01 g, 14.3 mmol) followed by a solution of tert-butyl(chloro)dimethylsilane (2.63 ml, 13.7 mmol) in dichloromethane (10 ml) dropwise. The resulting white suspension was stirred for 16 hours at room temperature before concentrating in vacuo. The residue was diluted with ethyl acetate (20 ml) and water (20 ml). The aqueous phase was acidified with hydrochloric acid (2 M aqueous solution) and extracted with ethyl acetate. The combined organic layers were washed with hydrochloric acid (2 M aqueous solution), saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel column) eluting with ethyl acetate:heptane (gradient 0:1 to 3:7, by volume) to afford the title compound as pale yellow oil, 2.2 g, 95% yield.

Quelle