Reaktion #43530

ord-303c601ec63140ad9cb114983ef5fc0e

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added dropwise at 0° C.
  2. 2
    Sonstigeto the reaction liquid
  3. 3
    Trocknendried with anhydrous magnesium sulfate
  4. 4
    SonstigeResidues obtained by the removal of solvent
  5. 5
    Sonstigewere purified by silica gel column chromatography

Vorschrift

Subsequently, 2.76 g (14.4 mmol) of 3,5-bis(methoxymethyl)styrene was dissolved in 30 ml of carbon tetrachloride in a reaction vessel of 200 ml, then 40 ml of methylene chloride solution containing 1.0 M boron trichloride was added dropwise at 0° C., and further agitated at 0° C. for 12 hours. After treating the excess boron trichloride by adding methanol to the reaction liquid, the resultant was poured into 150 ml of 5% NaOH solution (added with 100 g of ice). The organic layer was aliquoted and dried with anhydrous magnesium sulfate. Residues obtained by the removal of solvent were purified by silica gel column chromatography to obtain 1.57 g (7.81 mmol) of the target 3,5-bis(chloromethyl)styrene as a transparent liquid. Yield was 54%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732549B2uspto-grants-2010_06