Reaktion #2045050

ord-8f48782a75f947b0928a27e00baa35d7

Reaktionsgleichung

O=C(Cl)COCc1ccccc1
Benzyloxyacetyl chloride
COC(=O)CCCCCOc1ccc(N)cc1
6-(4-aminophenoxy)hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(N)cc1
6-(4-Amino-phenoxy)-hexanoic acid methyl ester
CCN(CC)CC
triethylamine
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
70
Ausbeute 22.2%
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
6-[4-(2-Benzyloxyacetylamino)phenoxy]hexanoic acid methyl ester
Ausbeute 22.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationSolids were filtered off
  2. 2
    workup.DISTILLATIONacetone distilled off
  3. 3
    workup.ADDITIONwater (100 ml) added
  4. 4
    ExtraktionCrude 70 was extracted into chloroform
  5. 5
    Waschenwashed with 5% sodium bicarbonate solution (2×100 ml), water (100 ml)
  6. 6
    Trocknendried over sodium sulphate
  7. 7
    workup.DISTILLATIONdistilled
  8. 8
    SonstigeCrude 70 was purified by column chromatography on silica gel

Vorschrift

Benzyloxyacetyl chloride (25 gm, 135.5 mmol) was added dropwise to a mixture of 6-(4-aminophenoxy)hexanoic acid methyl ester 21 (25 g, 105 mmol) and triethylamine (21.4 g, 211.6 mmol) in acetone (200 ml) at 0° C. and stirred at room temp. for 12 hrs. Solids were filtered off, acetone distilled off and water (100 ml) added. Crude 70 was extracted into chloroform, washed with 5% sodium bicarbonate solution (2×100 ml), water (100 ml), dried over sodium sulphate and distilled. Crude 70 was purified by column chromatography on silica gel using benzene as eluant to get pure 70 (9 g, 22.2%) as a off-white powder. M.p: 46-49° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08409559B2uspto-grants-2013_04