Реакция #429845

ord-51117ebb90784b06b3c459b6822624f2

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwhile being cooled with ice
  2. 2
    workup.STIRRINGwas stirred for 1.5 hours at room temperature
  3. 3
    ПромывкаThe reaction mixture was washed with saturated sodium hydrogencarbonate aqueous solution and saturated brine successively
  4. 4
    Сушкаdried over sodium sulfate anhydride
  5. 5
    Концентрированиеconcentrated under a vacuum
  6. 6
    ДругоеThe residue was purified by silica gel column chromatography (chloroform:methanol=40:1)
  7. 7
    ДругоеThe resulting solid was recrystallized from n-hexane/ethyl acetate

Методика

4-geranyloxybenzoic acid(1.37 g) was dissolved in chloroform(30 ml) and triethylamine(1.53 ml), and then diphenylphosphinic chloride(1.05 ml) was added thereto while being cooled with ice. After being stirred for 30 minutes, the mixture, with 2-(2-aminoethyl)pyridine(0.67 g) added thereto, was stirred for 1.5 hours at room temperature. The reaction mixture was washed with saturated sodium hydrogencarbonate aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and then concentrated under a vacuum. The residue was purified by silica gel column chromatography (chloroform:methanol=40:1). The resulting solid was recrystallized from n-hexane/ethyl acetate, thereby yielding 1.39 g of the aimed compound.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05859032uspto-grants-1999_01