Reacción #2355138

ord-a81c024108954c3da6b384adb0a4da93

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONUpon completion of the addition the reaction mixture
  2. 2
    FiltraciónAfter this time the reaction mixture was filtered
  3. 3
    Concentraciónconcentrated under reduced pressure
  4. 4
    Concentraciónconcentrated under reduced pressure

Procedimiento

A stirred solution of 9.0 grams (0.036 mole) of (2-chlorophenyl)(4-chlorophenyl)methanol in 90 mL of chloroform was cooled to 0° C., and 5.3 mL (0.072 mole) of thionyl chloride was added. Upon completion of the addition the reaction mixture was allowed to warm to ambient temperature, where it stirred for about 18 hours. After this time the reaction mixture was filtered and concentrated under reduced pressure. The filtrate was taken up in hexane and subjected to column chromatography on silica gel with hexane as eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 10.0 grams of (2-chlorophenyl)(4-chlorophenyl)methyl chloride. The NMR spectrum was consistent with the proposed structure.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USH0002007H1uspto-grants-2001_12