Reaktion #76091

ord-b75929fa69b14ec29f4afa3640ccb525

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was warmed to room temperature
  2. 2
    TemperaturThe mixture was cooled to −78° C.
  3. 3
    TemperaturThe mixture was warmed to room temperature
  4. 4
    workup.STIRRINGstirred for 20 minutes
  5. 5
    Extraktionextracted with dichloromethane (3×)
  6. 6
    Trocknendried over anhydrous sodium sulfate
  7. 7
    Einengenconcentrated to a clear film
  8. 8
    workup.DISSOLUTIONThis was dissolved in dioxane/2M HCl (10 mL/10 mL)
  9. 9
    Temperaturwas refluxed for 20 minutes
  10. 10
    TemperaturThe mixture was cooled
  11. 11
    WaschenThe basic solution was washed with diethyl ether (3×)
  12. 12
    ExtraktionThe acidic solution was extracted with diethyl ether (3×)
  13. 13
    Waschenwashed with brine (2×)
  14. 14
    Trocknendried over anhydrous sodium sulfate
  15. 15
    Einengenconcentrated

Vorschrift

To a solution of the impure 3-[4-(2-heptylamino-ethyl)-phenyl]-2,2-dimethyl-propionic acid ethyl ester (100 mg of the mixture) dissolved in methylene chloride (5 mL) cooled to −78° C. under a nitrogen atmosphere was added boron tribromide (1M in dichloromethane, 0.432 mL). The mixture was warmed to room temperature and stirred for 3 h. The mixture was cooled to −78° C. and an additional 0.432 mL of the 1M boron tribromide in dichloromethane was added. The mixture was warmed to room temperature and stirred for 20 minutes. The mixture was poured over H2O (10 mL) and extracted with dichloromethane (3×). The organic layers were combined, dried over anhydrous sodium sulfate, and concentrated to a clear film. This was dissolved in dioxane/2M HCl (10 mL/10 mL) and was refluxed for 20 minutes. The mixture was cooled and brought to pH 10 with 2 N NaOH. The basic solution was washed with diethyl ether (3×) and brought to pH 4 with 2N HCL. The acidic solution was extracted with diethyl ether (3×), washed with brine (2×), dried over anhydrous sodium sulfate and concentrated to give 3-[4-(2-heptylamino-ethyl)-phenyl]-2,2-dimethyl-propionic acid as a clear film (23 mg, 46%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06699904B2uspto-grants-2004_03