Reaktion #165056

ord-67da081b261c4fff94c37c31a6fe9f30

Reaktionsgleichung

OCc1cccc(Oc2ccccc2)c1
(3-phenoxy-phenyl)-methanol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
ClC(Cl)(Cl)Cl
carbon tetrachloride
ClCc1cccc(Oc2ccccc2)c1
title compound
Ausbeute 94.0%
ClCc1cccc(Oc2ccccc2)c1
1-Chloromethyl-3-phenoxy-benzene
Ausbeute 94.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux
  2. 2
    Einengenconcentrated under a reduced pressure
  3. 3
    SonstigeThe residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1)

Vorschrift

To a solution of (3-phenoxy-phenyl)-methanol (2.00 g, 10.0 mmol) in carbon tetrachloride (40 mL) was added triphenylphosphine (3.15 g, 12.0 mmol) at room temperature. The reaction solution was stirred under nitrogen atmosphere for 5 hours and 40 minutes under reflux. The reaction mixture was cooled to room temperature and concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1) to obtain the title compound (2.05 g, 94%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08841327B2uspto-grants-2014_09