Reaktion #668153
ord-733498324b964a4ca206f6bfeb47655c
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigethe mercury salts removed by filtration
- 2Waschenwashed with ether
- 3ExtraktionThe filtrate was extracted with ether (3×100 ml)
- 4Waschenwashed with water (20 ml), saturated brine (20 ml)
- 5Trocknendried (MgSO4)
- 6Sonstigeevaporated
- 7SonstigeThe residue was purified by flash chromatography on silica gel using 10% ethyl acetate in toluene as eluent
Vorschrift
4-bromophenethyl bromide (4.0 g) was added in a dropwise manner to a cooled solution of methoxyethanol (50 ml) and mercury II perchlorate (prepared from 3.39 g of mercury II oxide and 4.71 g of 60% perchloric acid). The mixture was stirred overnight at ambient temperature. Saturated brine (80 ml) was added, the mercury salts removed by filtration and washed with ether. The filtrate was extracted with ether (3×100 ml). The ether extracts were combined, washed with water (20 ml), saturated brine (20 ml), dried (MgSO4) and evaporated. The residue was purified by flash chromatography on silica gel using 10% ethyl acetate in toluene as eluent to give 1-(-4-bromophenethyloxy)-2-methoxyethane (2.2 g) as a colourless oil; NMR(CDCl3): 2.8-2.9(2H,t), 3.4(3H,s), 3.5-3.6(4H,m), 3.6-3.75(2H,t 7.05-7.15(2H,d) and 7.35-7.45(2H,d).