Reaktion #214184

ord-04524262907b4d9296d172c0f7925759

Reaktionsgleichung

Oc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl
pentachlorophenol
CCO[Si](CCCN)(OCC)OCC
3-aminopropyltriethoxysilane
CCO[Si](CCCN)(OCC)Oc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl
3-aminopropyldiethoxypentachlorophenoxysilane

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeIn a 250 ml three-necked flask equipped with magnetic stirrer
  2. 2
    Temperaturreflux condenser
  3. 3
    Temperaturdrop by drop, with refluxing
  4. 4
    workup.WAITAfter three hours of boiling
  5. 5
    workup.STIRRINGstirring
  6. 6
    Einengenthe clear solution is concentrated
  7. 7
    workup.DISTILLATIONby distilling out the chloroform
  8. 8
    Sonstigethe ethanol that is formed
  9. 9
    Sonstigemost of the triethylamine, and the product is carefully precipitated with 130 ml of pentane
  10. 10
    workup.STIRRINGwith stirring
  11. 11
    WaschenIt is washed thrice with pentane
  12. 12
    Sonstigedecanted
  13. 13
    Sonstigedried in a high vacuum at about 60° C

Vorschrift

In a 250 ml three-necked flask equipped with magnetic stirrer, reflux condenser and dropping funnel, 26.6 g of pentachlorophenol is placed for dissolving in 70 ml of chloroform and 50 ml of triethylamine. Over a period of 10 minutes, 22.1 g of 3-aminopropyltriethoxysilane is added, drop by drop, with refluxing and stirring. After three hours of boiling and stirring, the clear solution is concentrated by distilling out the chloroform, the ethanol that is formed, and most of the triethylamine, and the product is carefully precipitated with 130 ml of pentane, with stirring. It is washed thrice with pentane and decanted, then dried in a high vacuum at about 60° C. 41 g of a finely divided 3-aminopropyldiethoxypentachlorophenoxysilane is obtained having a melting point of 122° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04254270uspto-grants-1981_03