Reaction #589051

ord-292e16187f924a95b9a0a705b3ed5f3e

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
62
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
    OtherThe catalyst was removed by filtration, and methanol
  2. 2
    workup.DISTILLATIONdistilled off
  3. 3
    OtherCrude 62 was purified by column chromatography on silica gel

Procedure

6-[4-(6-Benzyloxyhexanoylamino)-phenoxy]-hexanoic acid methyl ester 61 (10 g, 22.67 mmol) was dissolved in methanol (100 ml) in a pressure vessel. Palladium on carbon (5%, 6 grm) was added and the mixture stirred under a hydrogen atmosphere (4 kg) for 20 hrs. The catalyst was removed by filtration, and methanol distilled off. Crude 62 was purified by column chromatography on silica gel using chloroform as eluant to give pure 62 (5 g, 62.8%) as a white powder with a m.p. between 73-75.5° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07772352B2uspto-grants-2010_08