Reaktion #704791

Reaktionsgleichung

2-(4-benzyloxyphenyl)ethyl iodide

water

Diethyl ethylmalonate

sodium hydride

→

compound

Ausbeute 94.5%

Diethyl 2-ethyl-2-(2-(4-benzyloxyphenyl)ethyl)malonate

Ausbeute 94.5%

Lösungsmittel

dimethylformamide

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe whole mixture was stirred at 0° C. for 20 minutes
2. 2
   workup.WAITto stand at room temperature overnight
3. 3
   Extraktionextracted with ethyl acetate
4. 4
   WaschenThe ethyl acetate layer was washed with water
5. 5
   Trocknena saturated brine and dried over anhydrous magnesium sulfate
6. 6
   workup.DISTILLATIONThe solvent was distilled away under reduced pressure
7. 7
   Sonstigethe residue obtained
8. 8
   Sonstigewas purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:9)

Vorschrift

Diethyl ethylmalonate (50 g) was added to a suspension of sodium hydride (11 g) in dimethylformamide (200 ml) and tetrahydrofuran (50 ml), at 0° C., and the mixture was stirred at room temperature for 35 minutes. A solution of 2-(4-benzyloxyphenyl)ethyl iodide (90 g) was added to the reaction mixture at 0° C. and the whole mixture was stirred at 0° C. for 20 minutes and allowed to stand at room temperature overnight. The resultant mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and a saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:9) to give the subject compound (100 g).

Quelle