Réaction #725933

ord-bd4081c1094c4584837a87fa6f2920d5

Équation de réaction

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
Rendement 22.2%
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
6-[4-(2-Benzyloxyacetylamino)phenoxy]hexanoic acid methyl ester
Rendement 22.2%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07691364B2uspto-grants-2010_04