Reaktion #668153

ord-733498324b964a4ca206f6bfeb47655c

Reaktionsgleichung

O.[Cl-].[Na+]
brine
BrCCc1ccc(Br)cc1
4-bromophenethyl bromide
COC(C)O
methoxyethanol
COCCOCCc1ccc(Br)cc1
1-(-4-bromophenethyloxy)-2-methoxyethane

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe mercury salts removed by filtration
  2. 2
    Waschenwashed with ether
  3. 3
    ExtraktionThe filtrate was extracted with ether (3×100 ml)
  4. 4
    Waschenwashed with water (20 ml), saturated brine (20 ml)
  5. 5
    Trocknendried (MgSO4)
  6. 6
    Sonstigeevaporated
  7. 7
    SonstigeThe 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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05919793uspto-grants-1999_07