Реакция #1519094

ord-e565d9f02d4240609cdd5106b7ef50da

Уравнение реакции

ClCc1ccc(OCc2ccccc2)cc1
4-Benzyloxybenzyl chloride
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenyl phosphine
CCOCC
ether
[Cl-].c1ccc(COc2ccc(C[P+](c3ccccc3)(c3ccccc3)c3ccccc3)cc2)cc1
4-benzyloxybenzyltriphenyl phosphonium chloride

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe precipitated phosphonium salt was collected by filtration
  2. 2
    Промывкаrinsed with ether and air
  3. 3
    Другоеdried

Методика

4-Benzyloxybenzyl chloride (1 g, 0.0043 moles) and triphenyl phosphine (1.127 g, 1 equivalent) in anhydrous toluene (20 mL) were refluxed under nitrogen for ˜8-10 hours. A white precipitate appeared in the reaction mixture. The reaction mixture was then cooled to room temperature and ether (100 mL) was added. The precipitated phosphonium salt was collected by filtration, rinsed with ether and air dried. Yield=0.55 g (25%). MALDI-TOF MS 459.51 obs. (459.54 calc.).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07611909B1uspto-grants-2009_11