Reacción #320082

ord-002a73c05dcb4467af5ba441018d7825

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped with stirrer, condenser
  2. 2
    workup.ADDITIONare added dropwise over a period of 45 minutes
  3. 3
    OtroSolvent and excess bromide are removed in vacuo
  4. 4
    ExtracciónThe resulting solution is extracted three times with water
  5. 5
    SecadoThe organic phase is dried over sodium sulfate
  6. 6
    Otroevaporated to dryness

Procedimiento

A 1 l sulfonating flask equipped with stirrer, condenser, dropping funnel and internal thermometer is charged with 86.5 g (0.5 mol) of 4-bromophenol in 500 ml of methylcellosolve. After the mixture is heated to 60° C., 70.0 g of 30% NaOH (0.53 mol) are slowly run in. Stirring is continued for 15 minutes before 116.8 g (0.575 mol) of 3-bromomethylheptane are added dropwise over a period of 45 minutes. The reaction is continued overnight at 100° C. The thin-layer chromatogram shows almost quantitative conversion. Solvent and excess bromide are removed in vacuo, and the residue (oil) is taken up in 600 ml of toluene. The resulting solution is extracted three times with water. The organic phase is dried over sodium sulfate and evaporated to dryness to give 119.3 g (84% of theory) of 4-(2-ethylhexyloxy)bromobenzene as a light yellow oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05591850uspto-grants-1997_01