Reaction #2045055

ord-fb9a245a1c9f458ab96584e60ff128d5

Reaction equation

COC(=O)CCCCCOc1ccc(NC(=O)CCCCCOCc2ccccc2)cc1
6-[4-(6-Benzyloxyhexanoylamino)phenoxy]hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(NC(=O)CCCCCO)cc1
81
Yield 62.8%
COC(=O)CCCCCOc1ccc(NC(=O)CCCCCO)cc1
6-[4-(6-Hydroxyhexanoylamino)phenoxy]hexanoic acid methyl ester
Yield 62.8%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherCatalyst was removed by filtration and methanol
  2. 2
    workup.DISTILLATIONdistilled off
  3. 3
    OtherCrude 81 was purified by column chromatography on silica gel

Procedure

6-[4-(6-Benzyloxyhexanoylamino)phenoxy]hexanoic acid methyl ester 80 (10 g, 22.67 mmol) was dissolved in methanol (100 ml) in a pressure vessel, palladium on carbon (5%, 6 grams) added, and the mixture stirred under a hydrogen atm. (4 Kg) for 20 hrs. Catalyst was removed by filtration and methanol distilled off. Crude 81 was purified by column chromatography on silica gel using chloroform as eluant to give pure 81 (5 g, 62.8%) as a white powder. M.p: 73-75.5°

Source

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