반응 #1519094

ord-e565d9f02d4240609cdd5106b7ef50da

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The precipitated phosphonium salt was collected by filtration
  2. 2
    세척rinsed with ether and air
  3. 3
    기타dried

실험 절차

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.).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07611909B1uspto-grants-2009_11