Реакция #4413

ord-17ee4450157049288fbf93d876e000e4

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas refluxed for 5 hours
  2. 2
    ДругоеThe solvent was then removed under vacuum, 75 ml of water
  3. 3
    workup.ADDITIONwere added
  4. 4
    Экстракцияthe mixture was extracted with ether (3×150 ml)
  5. 5
    ЭкстракцияThe ether extract
  6. 6
    Другоеwas evaporated to an oil
  7. 7
    Другоеchromatographed on silica
  8. 8
    workup.DISSOLUTIONThe resulting yellow oil was dissolved in 150 ml of ether
  9. 9
    Другоеprecipitated with excess anhydrous hydrogen chloride

Методика

A mixture of 7.6 g of 1-(1-phenylethyl)piperazine, 3.2 g of 1-bromo-3-chloropropane and 50 ml of reagent ethanol was refluxed for 5 hours. The solvent was then removed under vacuum, 75 ml of water were added, and the mixture was extracted with ether (3×150 ml). The ether extract was evaporated to an oil and chromatographed on silica, the eluant being CH2Cl2 /CH3OH/ammonium hydroxide (45:5:1). The resulting yellow oil was dissolved in 150 ml of ether and precipitated with excess anhydrous hydrogen chloride to yield 6.1 g (51% of theory) of 1,3-bis[4-(1-phenylethyl) -1-piperazinyl]propane tetrahydrochloride. The product was recrystallized from ethanol/water to yield a white crystalline solid (m.p. 236°-246° C., with decomp.).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725597uspto-grants-1988_02