Reacción #2314277

ord-6a975dac1ff14d6da6746883679d4cec

Ecuación de reacción

COC(Cl)Cl
1,1-dichloromethl methy ether
CCCCCCCCCCCCc1ccccc1
n-dodecylbenzene
CCCCCCCCCCCCc1ccc(C=O)cc1
p-n-Dodecylbenzaldehyde
Rendimiento 40.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction system kept below 10° C. in an ice bath
  2. 2
    workup.STIRRINGfurther stirred at a room temperature for 45 minutes
  3. 3
    OtroThe resultant reaction mixture
  4. 4
    ExtracciónIt was extracted four times with 200 mL of dichloromethane
  5. 5
    Otrodried overnight on sodium sulfate
  6. 6
    OtroThe solvent was removed by the use of an evaporator
  7. 7
    Otropurified by column chromatography (silica gel, benzene:hexene =1:1)
  8. 8
    OtroConsequently, 11.22 g (40.2 mmol) of a light yellow slightly viscous liquid was obtained

Procedimiento

To 70 mL of dehydrated dichloromethane, 24.68 g (100 mmol) of n-dodecylbenzene was added and 36.82 g (189 mmol) of titanium tetrachloride was gradually added in drops. The reaction system kept below 10° C. in an ice bath and 13.16 9 (114 mmol) of 1,1-dichloromethl methy ether added in drops thereto were stirred together below 10° C. for 30 minutes and further stirred at a room temperature for 45 minutes. The resultant reaction mixture was added to 500 mL of ice water. It was extracted four times with 200 mL of dichloromethane and dried overnight on sodium sulfate. The solvent was removed by the use of an evaporator and purified by column chromatography (silica gel, benzene:hexene =1:1). Consequently, 11.22 g (40.2 mmol) of a light yellow slightly viscous liquid was obtained. The yield was 40%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06413447B1uspto-grants-2002_07